GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS
K-Number: K930496 · 1993-04-20
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Device Summary
Frequently Asked Questions
What is the GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS?
GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Birtcher Medical Systems, Inc.. The 510(k) number is K930496.
When did GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS receive FDA 510(k) clearance?
GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS received FDA 510(k) clearance on 1993-04-20, under 510(k) number K930496.
Who is the listed applicant for GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS?
The FDA 510(k) record lists Birtcher Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS?
The FDA product code for GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPS is GCI.
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 Birtcher Medical Systems, 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: GCI)
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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