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FDA 510(k)

PROVAC WOUND HEALING/SUCTION SET

K-Number: K850011 · 1985-05-21

ApplicantMedical Matrix, Inc.
Decision Date1985-05-21
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROVAC WOUND HEALING/SUCTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Matrix, Inc.. It received FDA 510(k) clearance on 1985-05-21 under 510(k) number K850011. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROVAC WOUND HEALING/SUCTION SET?

PROVAC WOUND HEALING/SUCTION SET is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Medical Matrix, Inc.. The 510(k) number is K850011.

When did PROVAC WOUND HEALING/SUCTION SET receive FDA 510(k) clearance?

PROVAC WOUND HEALING/SUCTION SET received FDA 510(k) clearance on 1985-05-21, under 510(k) number K850011.

Who is the listed applicant for PROVAC WOUND HEALING/SUCTION SET?

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

What is the FDA product code for PROVAC WOUND HEALING/SUCTION SET?

The FDA product code for PROVAC WOUND HEALING/SUCTION SET is GCY.

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.

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Other records listing Medical Matrix, 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.

K850088ARTERIAL EXTENSION SET

Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

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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