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

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER

K Number: K812744 · Decision Dec 3, 1981
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
17
Review Days
65

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Basic Information

Device Name
LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER
K Number
K812744
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Progress Mankind Technology
Date Received
September 29, 1981
Decision Date
December 3, 1981
Product Code
HAW
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
HAW Neurological Stereotaxic Instrument

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