FDA 510(k) Substantially Equivalent 🇺🇸 United States

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV

K Number: K820334 · Decision Mar 15, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
13
Review Days
38

Basic Information

Device Name
NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV
K Number
K820334
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
NEMECTRON MEDICAL, INC.
Date Received
February 5, 1982
Decision Date
March 15, 1982
Advisory Committee
Unknown
Review Advisory Committee
NE
Third Party
N

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Search all 13 clearances from NEMECTRON MEDICAL, INC. →