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

MODIFIED AIR FLUIDIZED BED, KINAIR

K Number: K880340 · Decision Feb 16, 1988
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
27
Applicant Total
48
Review Days
21

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Basic Information

Device Name
MODIFIED AIR FLUIDIZED BED, KINAIR
K Number
K880340
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5160
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Kinetic Concepts, Inc.
Date Received
January 26, 1988
Decision Date
February 16, 1988
Product Code
INX
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
INX Bed, Air Fluidized

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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. →