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FDA 510(k)

ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID

K-Number: K040282 · 2004-04-29

Decision Date2004-04-29
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Internacional Farmaceutica, S.A. DE C.V.. It received FDA 510(k) clearance on 2004-04-29 under 510(k) number K040282. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID?

ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID is a medical device that received FDA 510(k) clearance on 2004-04-29. The listed applicant is Internacional Farmaceutica, S.A. DE C.V.. The 510(k) number is K040282.

When did ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID receive FDA 510(k) clearance?

ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID received FDA 510(k) clearance on 2004-04-29, under 510(k) number K040282.

Who is the listed applicant for ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID?

The FDA 510(k) record lists Internacional Farmaceutica, S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID?

The FDA product code for ATRAMAT AND SORB-FAST POLYGLYCOLIC ACID 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 Internacional Farmaceutica, S.A. DE C.V. 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 10 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

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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