FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM

K Number: K873332 · Decision Sep 8, 1987
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
95
Applicant Total
31
Review Days
20

Basic Information

Device Name
MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
K Number
K873332
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
AMERICAN V. MUELLER
Date Received
August 19, 1987
Decision Date
September 8, 1987
Product Code
GCY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

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