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FDA 510(k)

USSC MONOFILAMENT POLYSORB SUTURE

K-Number: K945285 · 1995-08-21

Decision Date1995-08-21
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

USSC MONOFILAMENT POLYSORB SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1995-08-21 under 510(k) number K945285. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the USSC MONOFILAMENT POLYSORB SUTURE?

USSC MONOFILAMENT POLYSORB SUTURE is a medical device that received FDA 510(k) clearance on 1995-08-21. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K945285.

When did USSC MONOFILAMENT POLYSORB SUTURE receive FDA 510(k) clearance?

USSC MONOFILAMENT POLYSORB SUTURE received FDA 510(k) clearance on 1995-08-21, under 510(k) number K945285.

Who is the listed applicant for USSC MONOFILAMENT POLYSORB SUTURE?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for USSC MONOFILAMENT POLYSORB SUTURE?

The FDA product code for USSC MONOFILAMENT POLYSORB 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 United States Surgical, A Division of Tyco Healthc 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.

View all 218 devices →

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

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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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