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FDA 510(k)

STERILE POLYHESIVE PBS DRESSING

K-Number: K890021 · 1989-06-01

Decision Date1989-06-01
Product CodeKGF
DecisionSubstantially Equivalent for Some Indications

Device Summary

STERILE POLYHESIVE PBS DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1989-06-01 under 510(k) number K890021. The device is classified under product code KGF. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the STERILE POLYHESIVE PBS DRESSING?

STERILE POLYHESIVE PBS DRESSING is a medical device that received FDA 510(k) clearance on 1989-06-01. The listed applicant is Valleylab, Inc.. The 510(k) number is K890021.

When did STERILE POLYHESIVE PBS DRESSING receive FDA 510(k) clearance?

STERILE POLYHESIVE PBS DRESSING received FDA 510(k) clearance on 1989-06-01, under 510(k) number K890021.

Who is the listed applicant for STERILE POLYHESIVE PBS DRESSING?

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

What is the FDA product code for STERILE POLYHESIVE PBS DRESSING?

The FDA product code for STERILE POLYHESIVE PBS DRESSING is KGF.

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 Valleylab, 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.

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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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