FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

BLY-501 ADAPTOR

K Number: K012540 · Decision Sep 26, 2001
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
6
Review Days
50

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Basic Information

Device Name
BLY-501 ADAPTOR
K Number
K012540
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micromedical Industries, Ltd.
Date Received
August 7, 2001
Decision Date
September 26, 2001
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DPS Electrocardiograph

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K915624 MODIFIED BIOLOG