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

CARDIOLIGHT

K Number: K982448 · Decision Jun 11, 1999
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
14
Review Days
331

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Basic Information

Device Name
CARDIOLIGHT
K Number
K982448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Capintec, Inc.
Date Received
July 15, 1998
Decision Date
June 11, 1999
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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