VICRYL RAPIDE SUTURE
K-Number: K944110 · 1995-01-18
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Device Summary
Frequently Asked Questions
What is the VICRYL RAPIDE SUTURE?
VICRYL RAPIDE SUTURE is a medical device that received FDA 510(k) clearance on 1995-01-18. The listed applicant is ETHICON, Inc.. The 510(k) number is K944110.
When did VICRYL RAPIDE SUTURE receive FDA 510(k) clearance?
VICRYL RAPIDE SUTURE received FDA 510(k) clearance on 1995-01-18, under 510(k) number K944110.
Who is the listed applicant for VICRYL RAPIDE SUTURE?
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 VICRYL RAPIDE SUTURE?
The FDA product code for VICRYL RAPIDE SUTURE is GAM.
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: GAM)
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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