STRYKER ENDOSCOPY CHOLANGIOGRAM KIT
K-Number: K924212 · 1993-07-07
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Device Summary
Frequently Asked Questions
What is the STRYKER ENDOSCOPY CHOLANGIOGRAM KIT?
STRYKER ENDOSCOPY CHOLANGIOGRAM KIT is a medical device that received FDA 510(k) clearance on 1993-07-07. The listed applicant is Stryker Corp.. The 510(k) number is K924212.
When did STRYKER ENDOSCOPY CHOLANGIOGRAM KIT receive FDA 510(k) clearance?
STRYKER ENDOSCOPY CHOLANGIOGRAM KIT received FDA 510(k) clearance on 1993-07-07, under 510(k) number K924212.
Who is the listed applicant for STRYKER ENDOSCOPY CHOLANGIOGRAM KIT?
The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER ENDOSCOPY CHOLANGIOGRAM KIT?
The FDA product code for STRYKER ENDOSCOPY CHOLANGIOGRAM KIT is GBZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Stryker Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GBZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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