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

WET CHAMBER

K Number: K020781 · Decision May 6, 2002
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
48
Review Days
56

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Basic Information

Device Name
WET CHAMBER
K Number
K020781
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kinetic Concepts, Inc.
Date Received
March 11, 2002
Decision Date
May 6, 2002
Product Code
NAD
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
NAD Dressing, Wound, Occlusive

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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
K992448 V.A.C. PLUS
K972176 HOME CARE BEAD BED
K972549 SIMPULSE
K955243 BARIAIR
Search all 48 clearances from Kinetic Concepts, Inc. →