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

THE POREX RETRACTOR TABLE

K Number: K860503 · Decision Mar 13, 1986
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
12
Applicant Total
15
Review Days
30

Basic Information

Device Name
THE POREX RETRACTOR TABLE
K Number
K860503
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
POREX MEDICAL
Date Received
February 11, 1986
Decision Date
March 13, 1986
Product Code
FSE
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
FSE Table, Operating-Room, Manual

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Other Clearances by POREX MEDICAL

K Number Device Name
K872791 POREX NERVE LOCATOR
K873044 POREX OTOLOGY INSTRUMENTS
K872947 POREX QUALITY PLASTIC SURGERY INSTRUMENTS
K863943 POREX(TM) EYE SPHERE IMPLANT
K863946 POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
K870182 POREX(TM) MALAR IMPLANT
K870257 POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.
K870154 POREX(TM) TISSUE EXPANDER
K863941 POREX(TM) PROSTHESIS, CHIN, INTERNAL
K863939 POREX(TM) EAR PROSTHESIS
Search all 15 clearances from POREX MEDICAL →