FDA 510(k) Unknown 🇺🇸 United States

GENERATOR, BIOTEC 876 PULSE

K Number: K790031 · Decision Jan 2, 1979
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
8
Review Days

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Basic Information

Device Name
GENERATOR, BIOTEC 876 PULSE
K Number
K790031
Clearance Type
Traditional
Decision
Unknown
Applicant
Biomagnetic Technologies, Inc.
Date Received
January 2, 1979
Decision Date
January 2, 1979
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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