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FDA 510(k)

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM

K-Number: K873332 · 1987-09-08

Decision Date1987-09-08
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1987-09-08 under 510(k) number K873332. 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 MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM?

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1987-09-08. The listed applicant is American V. Mueller. The 510(k) number is K873332.

When did MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM receive FDA 510(k) clearance?

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM received FDA 510(k) clearance on 1987-09-08, under 510(k) number K873332.

Who is the listed applicant for MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM?

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

What is the FDA product code for MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM?

The FDA product code for MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM 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.

Other records listing American V. Mueller 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 31 devices →

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.

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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