510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924212Unknown

Stryker Endoscopy Cholangiogram Kit

Stryker Corp., San Jose CA / Traditional, Unknown
FDA source (opens on fda.gov)

K924212 is the FDA 510(k) clearance record for STRYKER ENDOSCOPY CHOLANGIOGRAM KIT, a class I device, cleared for Stryker Corp. on under FDA product code GBZ (Catheter, Cholangiography). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show no recalls naming K924212.

Clearance record

Decision date
Received
(321 days to decision)
Product code
GBZ Catheter, Cholangiography
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Stryker Corp. 210 Baypointe Pkwy., San Jose CA
510(k) summary
Statement
Third party review
No

Clearances, product code GBZ

Trailing 12 months

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

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