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FDA 510(k)

SUTRALON NYLON SUTURES

K-Number: K994176 · 2000-02-08

Decision Date2000-02-08
Product CodeGAR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTRALON NYLON SUTURES is the device name listed in this FDA 510(k) record. The listed applicant is Visionary Medical Supplies, Inc.. It received FDA 510(k) clearance on 2000-02-08 under 510(k) number K994176. 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 SUTRALON NYLON SUTURES?

SUTRALON NYLON SUTURES is a medical device that received FDA 510(k) clearance on 2000-02-08. The listed applicant is Visionary Medical Supplies, Inc.. The 510(k) number is K994176.

When did SUTRALON NYLON SUTURES receive FDA 510(k) clearance?

SUTRALON NYLON SUTURES received FDA 510(k) clearance on 2000-02-08, under 510(k) number K994176.

Who is the listed applicant for SUTRALON NYLON SUTURES?

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

What is the FDA product code for SUTRALON NYLON SUTURES?

The FDA product code for SUTRALON NYLON SUTURES 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 Visionary Medical Supplies, 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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