510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K951529Substantially Equivalent

V. Mueller Obstetrical (Ob) Forceps

Baxter Healthcare Corporation, Waukegan IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951529 is the FDA 510(k) clearance record for V. MUELLER OBSTETRICAL (OB) FORCEPS, a class II device, cleared for Baxter Healthcare Corp on under FDA product code HDA (Forceps, Obstetrical). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K951529.

Clearance record

Decision date
Received
(123 days to decision)
Product code
HDA Forceps, Obstetrical
Regulation
21 CFR 884.4400
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Baxter Healthcare Corp 1500 Waukegan Rd., Waukegan IL
510(k) summary
Summary
Third party review
No

Clearances, product code HDA

Trailing 12 months

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

FDA records show no clearances under product code HDA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HDA, 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