510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934235Substantially Equivalent

Sniff Position Pillow

American Medical Development, Inc., Boston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934235 is the FDA 510(k) clearance record for SNIFF POSITION PILLOW, a class I device, cleared for American Medical Development, Inc. on under FDA product code CCX (Support, Patient Position). FDA records list one 510(k) clearance for American Medical Development, Inc. As of , FDA records show no recalls naming K934235.

Clearance record

Decision date
Received
(32 days to decision)
Product code
CCX Support, Patient Position
Regulation
21 CFR 868.6820
Device class
Class I
Review panel
Anesthesiology
Applicant
American Medical Development, Inc. 220 Commercial St., Boston MA
510(k) summary
Statement
Third party review
No

Clearances, product code CCX

Trailing 12 months

FDA records hold no clearances under product code CCX in the trailing twelve months.

FDA records show no clearances under product code CCX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CCX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260