KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC
K-Number: K934937 · 1994-03-23
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Device Summary
Frequently Asked Questions
What is the KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC?
KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K934937.
When did KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC receive FDA 510(k) clearance?
KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC received FDA 510(k) clearance on 1994-03-23, under 510(k) number K934937.
Who is the listed applicant for KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC?
The FDA product code for KARL STORZ BIOP/BASK CUT/GRASP DISSEC/FLEX/CUT FORC is GCJ.
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 KARL STORZ Endoscopy-America, Inc. 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: GCJ)
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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