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FDA 510(k)

MICRINS MICROSURGICAL SUTURE

K-Number: K993970 · 2000-03-30

Decision Date2000-03-30
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRINS MICROSURGICAL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Micrins Surgical, Inc.. It received FDA 510(k) clearance on 2000-03-30 under 510(k) number K993970. The device is classified under product code GAR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRINS MICROSURGICAL SUTURE?

MICRINS MICROSURGICAL SUTURE is a medical device that received FDA 510(k) clearance on 2000-03-30. The listed applicant is Micrins Surgical, Inc.. The 510(k) number is K993970.

When did MICRINS MICROSURGICAL SUTURE receive FDA 510(k) clearance?

MICRINS MICROSURGICAL SUTURE received FDA 510(k) clearance on 2000-03-30, under 510(k) number K993970.

Who is the listed applicant for MICRINS MICROSURGICAL SUTURE?

The FDA 510(k) record lists Micrins Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRINS MICROSURGICAL SUTURE?

The FDA product code for MICRINS MICROSURGICAL SUTURE is GAR.

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 Micrins Surgical, 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: GAR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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