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FDA 510(k)

AEGIS NON-ADHERENT DRESSING

K-Number: K820413 · 1982-03-12

Decision Date1982-03-12
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AEGIS NON-ADHERENT DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Products, Inc.. It received FDA 510(k) clearance on 1982-03-12 under 510(k) number K820413. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEGIS NON-ADHERENT DRESSING?

AEGIS NON-ADHERENT DRESSING is a medical device that received FDA 510(k) clearance on 1982-03-12. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K820413.

When did AEGIS NON-ADHERENT DRESSING receive FDA 510(k) clearance?

AEGIS NON-ADHERENT DRESSING received FDA 510(k) clearance on 1982-03-12, under 510(k) number K820413.

Who is the listed applicant for AEGIS NON-ADHERENT DRESSING?

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

What is the FDA product code for AEGIS NON-ADHERENT DRESSING?

The FDA product code for AEGIS NON-ADHERENT DRESSING is NAB.

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 Professional Medical Products, 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.

View all 9 devices →

Related Devices (Code: NAB)

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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