FLEXIBLE SNARE
K-Number: K902265 · 1990-07-27
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE SNARE?
FLEXIBLE SNARE is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Annex Medical, Inc.. The 510(k) number is K902265.
When did FLEXIBLE SNARE receive FDA 510(k) clearance?
FLEXIBLE SNARE received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902265.
Who is the listed applicant for FLEXIBLE SNARE?
The FDA 510(k) record lists Annex Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE SNARE?
The FDA product code for FLEXIBLE SNARE is FDI.
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 Annex Medical, 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: FDI)
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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