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

V.A.C. ABDOMINAL DRESSING

K Number: K022011 · Decision Feb 26, 2003
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
48
Review Days
252

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Basic Information

Device Name
V.A.C. ABDOMINAL DRESSING
K Number
K022011
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetic Concepts, Inc.
Date Received
June 19, 2002
Decision Date
February 26, 2003
Product Code
FTL
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
FTL Mesh, Surgical, Polymeric

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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
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
K955243 BARIAIR
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