SNIFF POSITION PILLOW— 510(k) K934235

Name: FDA 510(k) clearance K934235
Creator: U.S. Food and Drug Administration
Published: 1993-10-01

Substantially Equivalent

American Medical Development, Inc.

FDA 510(k) clearance K934235 for SNIFF POSITION PILLOW, Substantially Equivalent on 1993-10-01. Applicant: American Medical Development, Inc.. Device class: 1.

Clearance details

Applicant: American Medical Development, Inc.
Product code: Code CCX
Device class: Class 1
Regulation: 21 CFR 868.6820
Advisory panel: Anesthesiology
Date received: 1993-08-30
Decision date: 1993-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boston, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.