GENICON CLIP APPLIER
K-Number: K030269 · 2003-03-20
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Device Summary
Frequently Asked Questions
What is the GENICON CLIP APPLIER?
GENICON CLIP APPLIER is a medical device that received FDA 510(k) clearance on 2003-03-20. The listed applicant is Genicon, LC. The 510(k) number is K030269.
When did GENICON CLIP APPLIER receive FDA 510(k) clearance?
GENICON CLIP APPLIER received FDA 510(k) clearance on 2003-03-20, under 510(k) number K030269.
Who is the listed applicant for GENICON CLIP APPLIER?
The FDA 510(k) record lists Genicon, LC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENICON CLIP APPLIER?
The FDA product code for GENICON CLIP APPLIER is FZP.
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 Genicon, LC 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: FZP)
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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