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

THE PORTABLE ORDERLY

K Number: K872900 · Decision Aug 21, 1987
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
60
Applicant Total
3
Review Days
28

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Basic Information

Device Name
THE PORTABLE ORDERLY
K Number
K872900
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Edgewater Medical Equipment Systems
Date Received
July 24, 1987
Decision Date
August 21, 1987
Product Code
FWZ
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
FWZ Operating Room Accessories Table Tray

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FWZ), ordered by most recent decision date.

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Other Clearances by Edgewater Medical Equipment Systems

K Number Device Name
K873370 ALLEN MALLEABLE ANESTHESIA SCREEN
K860177 ALLEN UNIVERSAL STIRRUP