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

PILLOW, CARTER ARM ELEVATION

K Number: K790283 · Decision Apr 6, 1979
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
64
Applicant Total
303
Review Days
52

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Basic Information

Device Name
PILLOW, CARTER ARM ELEVATION
K Number
K790283
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6060
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Depuy, Inc.
Date Received
February 13, 1979
Decision Date
April 6, 1979
Product Code
KME
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KME Bedding, Disposable, Medical

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