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FDA 510(k)

WOUND DRAINAGE MANAGEMENT SYSTEMS

K-Number: K813080 · 1981-11-17

Decision Date1981-11-17
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WOUND DRAINAGE MANAGEMENT SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1981-11-17 under 510(k) number K813080. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND DRAINAGE MANAGEMENT SYSTEMS?

WOUND DRAINAGE MANAGEMENT SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-11-17. The listed applicant is Howmedica Corp.. The 510(k) number is K813080.

When did WOUND DRAINAGE MANAGEMENT SYSTEMS receive FDA 510(k) clearance?

WOUND DRAINAGE MANAGEMENT SYSTEMS received FDA 510(k) clearance on 1981-11-17, under 510(k) number K813080.

Who is the listed applicant for WOUND DRAINAGE MANAGEMENT SYSTEMS?

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

What is the FDA product code for WOUND DRAINAGE MANAGEMENT SYSTEMS?

The FDA product code for WOUND DRAINAGE MANAGEMENT SYSTEMS is EXB.

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 Howmedica Corp. 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 373 devices →

Related Devices (Code: EXB)

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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