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FDA 510(k)

SOLCOVAC WOUND DRAINAGE SYSTEM

K-Number: K915867 · 1992-08-14

ApplicantSolco Basle, Inc.
Decision Date1992-08-14
Product CodeGCY
Advisory CommitteeSU
DecisionUnknown

Device Summary

SOLCOVAC WOUND DRAINAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Solco Basle, Inc.. It received FDA 510(k) clearance on 1992-08-14 under 510(k) number K915867. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SOLCOVAC WOUND DRAINAGE SYSTEM?

SOLCOVAC WOUND DRAINAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1992-08-14. The listed applicant is Solco Basle, Inc.. The 510(k) number is K915867.

When did SOLCOVAC WOUND DRAINAGE SYSTEM receive FDA 510(k) clearance?

SOLCOVAC WOUND DRAINAGE SYSTEM received FDA 510(k) clearance on 1992-08-14, under 510(k) number K915867.

Who is the listed applicant for SOLCOVAC WOUND DRAINAGE SYSTEM?

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

What is the FDA product code for SOLCOVAC WOUND DRAINAGE SYSTEM?

The FDA product code for SOLCOVAC WOUND DRAINAGE SYSTEM is GCY.

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Other records listing Solco Basle, 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.

K913247SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEMK913177SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEMK896858SOLCOTRANS INTRAOPERATIVE AUTOTRANSFUSION SYSTEMK896857SOLCOTRANS ORTHOPAEDIC DRAINAGE/REINFUSION SYSTEMK896203SOLCOSEPT(TM) BLOOD TRANSFUSION FILTERK883058SOLCOTRANS ORTHO. DRAINAGE/REINFUSION SYSTEM

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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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