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

POREX NERVE LOCATOR

K Number: K872791 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
96
Applicant Total
15
Review Days
98

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Basic Information

Device Name
POREX NERVE LOCATOR
K Number
K872791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Porex Medical
Date Received
July 14, 1987
Decision Date
October 20, 1987
Product Code
ETN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ETN Stimulator, Nerve

Similar 510(k) Clearances

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Other Clearances by Porex Medical

K Number Device Name
K873044 POREX OTOLOGY INSTRUMENTS
K872947 POREX QUALITY PLASTIC SURGERY INSTRUMENTS
K863943 POREX(TM) EYE SPHERE IMPLANT
K863946 POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
K870154 POREX(TM) TISSUE EXPANDER
K870182 POREX(TM) MALAR IMPLANT
K870257 POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.
K863939 POREX(TM) EAR PROSTHESIS
K863942 POREX(TM) NOSE PROSTHESIS
K863941 POREX(TM) PROSTHESIS, CHIN, INTERNAL
Search all 15 clearances from Porex Medical →