510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K072702Substantially Equivalent

Stryker Antimic Catheter

Stryker Corp., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072702 is the FDA 510(k) clearance record for STRYKER ANTIMIC CATHETER, a class II device, cleared for Stryker Instruments, Instruments Div. on under FDA product code BSO (Catheter, Conduction, Anesthetic). FDA records list 568 510(k) clearances for STRYKER CORP., from to . As of , FDA records show no recalls naming K072702.

Clearance record

Decision date
Received
(177 days to decision)
Product code
BSO Catheter, Conduction, Anesthetic
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Stryker Instruments, Instruments Div. 4100 E. Milham Ave., Kalamazoo MI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BSO

Trailing 12 months

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

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