510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760175Substantially Equivalent

Drape, Transurethral Resection (Tur)

V. Mueller O.V. Baxter Healthcare Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760175 is the FDA 510(k) clearance record for DRAPE, TRANSURETHRAL RESECTION (TUR), a class II device, cleared for V. Mueller O.V. Baxter Healthcare Corp. on under FDA product code EYX (Drape, Pure Latex Sheet, With Self-Retaining Finger Cot). FDA records list 41 510(k) clearances for V. Mueller O.V. Baxter Healthcare Corp., from to . As of , FDA records show no recalls naming K760175.

Clearance record

Decision date
Received
(55 days to decision)
Product code
EYX Drape, Pure Latex Sheet, With Self-Retaining Finger Cot
Regulation
21 CFR 878.4370
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
V. Mueller O.V. Baxter Healthcare Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EYX

Trailing 12 months

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

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