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FDA 510(k)

AEROPLAST DRESSING

K-Number: K781031 · 1978-07-27

ApplicantParke-Davis Co.
Decision Date1978-07-27
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AEROPLAST DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K781031. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROPLAST DRESSING?

AEROPLAST DRESSING is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Parke-Davis Co.. The 510(k) number is K781031.

When did AEROPLAST DRESSING receive FDA 510(k) clearance?

AEROPLAST DRESSING received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781031.

Who is the listed applicant for AEROPLAST DRESSING?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AEROPLAST DRESSING?

The FDA product code for AEROPLAST DRESSING is KMF.

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Related Devices (Code: KMF)

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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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