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

MODEL 1301 BIOTAC (TM)

K Number: K810627 · Decision Apr 2, 1981
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
17
Review Days
24

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Basic Information

Device Name
MODEL 1301 BIOTAC (TM)
K Number
K810627
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Progress Mankind Technology
Date Received
March 9, 1981
Decision Date
April 2, 1981
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

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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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