MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
K-Number: K873332 · 1987-09-08
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Device Summary
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.
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
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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