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

PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC

K Number: K802151 · Decision Nov 19, 1980
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
57
Applicant Total
17
Review Days
72

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Basic Information

Device Name
PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC
K Number
K802151
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1330
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Progress Mankind Technology
Date Received
September 8, 1980
Decision Date
November 19, 1980
Product Code
GZL
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZL Electrode, Depth

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K871663 PMT TRACTION TONGS
K854157 PMT ACCUPRESSURE INFUSION SYSTEM 3601
K845035 ELECTRODE FOR NEUROLOGICAL SURGERY 2111
K845036 TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600
K834047 PMT-HALO/ORTHOPEDIC JACKET SYSTEM
K831329 PMT VAXIOM STEREOTACTIC SYS #FX001
K830530 TEMP TRACE
K812744 LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER
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