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

PORTABLE CLOSED WOUND SUCTION EVACUATOR

K Number: K780848 · Decision Aug 23, 1978
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
441
Review Days
92

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Basic Information

Device Name
PORTABLE CLOSED WOUND SUCTION EVACUATOR
K Number
K780848
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Biomet, Inc.
Date Received
May 23, 1978
Decision Date
August 23, 1978
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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