Medical Devices; Exemption From Premarket Notification: Powered Patient Transport, All Other Powered Patient Transport

---
identifier: "/us/fr/2021-13967"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Medical Devices; Exemption From Premarket Notification: Powered Patient Transport, All Other Powered Patient Transport"
title_number: 0
title_name: "Federal Register"
section_number: "2021-13967"
section_name: "Medical Devices; Exemption From Premarket Notification: Powered Patient Transport, All Other Powered Patient Transport"
positive_law: false
currency: "2021-06-30"
last_updated: "2021-06-30"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "2021-13967"
document_type: "notice"
publication_date: "2021-06-30"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "86 FR 34770"
fr_volume: 86
docket_ids:
  - "Docket No. FDA-2021-P-0424"
fr_action: "Notice; correction."
---


#  Medical Devices; Exemption From Premarket Notification: Powered Patient Transport, All Other Powered Patient Transport

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; correction.

**SUMMARY:**

The Food and Drug Administration (FDA) is correcting a notice announcing receipt of a petition requesting exemption from the premarket notification requirements. The document was published with an incorrect docket number. This document corrects that error.

**FOR FURTHER INFORMATION CONTACT:**

Dan Reed, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 1526, Silver Spring, MD 20993-0002, 240-402-4717.

**SUPPLEMENTARY INFORMATION:**

In the *Federal Register* of June 15, 2021 (86 FR 31722), in FR Doc. 2021-12505, on page 31722, the following correction is made:

On page 31722, in the second column, in the header of the document, and, also on page 31723, in the first column under “Instructions,” “Docket No. FDA-2021-N-0493” is corrected to read “Docket No. FDA-2021-P-0424”.

Dated: June 25, 2021.

Lauren K. Roth,

Acting Principal Associate Commissioner for Policy.