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

3 CHANNEL DIGITAL AMBULATORY ECG RECORDER

K Number: K971670 · Decision Jan 29, 1998
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
6
Review Days
268

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Basic Information

Device Name
3 CHANNEL DIGITAL AMBULATORY ECG RECORDER
K Number
K971670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Galix Biomedical Instrumentation, Inc.
Date Received
May 6, 1997
Decision Date
January 29, 1998
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DSH), ordered by most recent decision date.

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Other Clearances by Galix Biomedical Instrumentation, Inc.

K Number Device Name
K092853 3 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SM
K051163 GALIX ECG PROFESSIONAL STATION
K030145 GALIX WINTER
K023080 GALIX PACESTAR
K992706 GALIX GBI -3S-LP