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

QUICKSCAN HOLTER II

K Number: K790476 · Decision Jun 1, 1979
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
17
Review Days
88

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Basic Information

Device Name
QUICKSCAN HOLTER II
K Number
K790476
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intl. Medical, Inc.
Date Received
March 5, 1979
Decision Date
June 1, 1979
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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