510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760183Substantially Equivalent

Obturator, Deflecting

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

K760183 is the FDA 510(k) clearance record for OBTURATOR, DEFLECTING, a class II device, cleared for V. Mueller O.V. Baxter Healthcare Corp. on under FDA product code FEC (Obturator, For Endoscope). 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 K760183.

Clearance record

Decision date
Received
(149 days to decision)
Product code
FEC Obturator, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
V. Mueller O.V. Baxter Healthcare Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FEC

Trailing 12 months

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

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