510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903744Substantially Equivalent

Physician's Choice

Advance Medical Device, Inc., Ontario L3y 4v8, Canada, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K903744 is the FDA 510(k) clearance record for PHYSICIAN'S CHOICE, a class II device, cleared for Advance Medical Device, Inc. on under FDA product code HIB (Speculum, Vaginal, Nonmetal). FDA records list 5 510(k) clearances for Advance Medical Device, Inc., from to . As of , FDA records show no recalls naming K903744.

Clearance record

Decision date
Received
(27 days to decision)
Product code
HIB Speculum, Vaginal, Nonmetal
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Advance Medical Device, Inc. 15 Valley Trl.,, Ontario L3y 4v8, Canada, CA
Third party review
No

Clearances, product code HIB

Trailing 12 months
1 clearance under product code HIB in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HIB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260