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FDA 510(k)

VIGILON PRIMARY WOUND DRESSING, STERILE

K-Number: K820134 · 1982-02-05

ApplicantC.R. Bard, Inc.
Decision Date1982-02-05
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIGILON PRIMARY WOUND DRESSING, STERILE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820134. 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 VIGILON PRIMARY WOUND DRESSING, STERILE?

VIGILON PRIMARY WOUND DRESSING, STERILE is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K820134.

When did VIGILON PRIMARY WOUND DRESSING, STERILE receive FDA 510(k) clearance?

VIGILON PRIMARY WOUND DRESSING, STERILE received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820134.

Who is the listed applicant for VIGILON PRIMARY WOUND DRESSING, STERILE?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIGILON PRIMARY WOUND DRESSING, STERILE?

The FDA product code for VIGILON PRIMARY WOUND DRESSING, STERILE is 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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