510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K911606Unknown

Baxter Preoperative Skin Prep Tray W/foam Sponges

Baxter Healthcare Corporation, Valencia CA / Traditional, Unknown
FDA source (opens on fda.gov)

K911606 is the FDA 510(k) clearance record for BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES, a class I device, cleared for Baxter Healthcare Corp on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 570 510(k) clearances for Baxter Healthcare Corp, from to . As of , FDA records show no recalls naming K911606.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Baxter Healthcare Corp 27200 N. Tourney Rd., Valencia CA
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

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