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

MODEL 500 PEDIATRIC STRETCHER/CRIB

K Number: K852422 · Decision Jul 5, 1985
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
26
Applicant Total
31
Review Days
28

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Basic Information

Device Name
MODEL 500 PEDIATRIC STRETCHER/CRIB
K Number
K852422
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5140
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Midmark Corp.
Date Received
June 7, 1985
Decision Date
July 5, 1985
Product Code
FMS
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
FMS Bed, Pediatric Open Hospital

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