FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VACPLUS

K Number: K945062 · Decision Mar 14, 1995
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
48
Review Days
151

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Basic Information

Device Name
VACPLUS
K Number
K945062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kinetic Concepts, Inc.
Date Received
October 14, 1994
Decision Date
March 14, 1995
Product Code
JCX
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
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

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Other Clearances by Kinetic Concepts, Inc.

K Number Device Name
K050261 V.A.C. GRANUFOAM SILVER PROTECTION DRESSING
K041642 V.A.C. GRANUFOAM SILVER DRESSING
K032310 MINI V.A.C., V.A.C. FREEDOM, V.A.C. ATS
K022011 V.A.C. ABDOMINAL DRESSING
K021500 VACUUM ASSISTED CLOSURE
K021501 V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT
K020781 WET CHAMBER
K992448 V.A.C. PLUS
K972176 HOME CARE BEAD BED
K972549 SIMPULSE
Search all 48 clearances from Kinetic Concepts, Inc. →