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

WEIGHMOBILE, IN BED PATIENT WEIGHING SCALE

K Number: K864953 · Decision Jan 21, 1987
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
47
Applicant Total
2
Review Days
34

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Basic Information

Device Name
WEIGHMOBILE, IN BED PATIENT WEIGHING SCALE
K Number
K864953
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.2720
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Dittmar and Penn Corp.
Date Received
December 18, 1986
Decision Date
January 21, 1987
Product Code
FRW
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
FRW Scale, Patient

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K Number Device Name
K883260 DITTMAR POWER LIFTER