LIGACLIP MULTIPLE CLIP APPLIER
K-Number: K771412 · 1977-11-28
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Device Summary
Frequently Asked Questions
What is the LIGACLIP MULTIPLE CLIP APPLIER?
LIGACLIP MULTIPLE CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is ETHICON, Inc.. The 510(k) number is K771412.
When did LIGACLIP MULTIPLE CLIP APPLIER receive FDA 510(k) clearance?
LIGACLIP MULTIPLE CLIP APPLIER received FDA 510(k) clearance on 1977-11-28, under 510(k) number K771412.
Who is the listed applicant for LIGACLIP MULTIPLE CLIP APPLIER?
The FDA 510(k) record lists ETHICON, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGACLIP MULTIPLE CLIP APPLIER?
The FDA product code for LIGACLIP MULTIPLE CLIP APPLIER is GDO.
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 ETHICON, 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: GDO)
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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