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

NIGHTWATCH(TM) SYSTEM

K Number: K870578 · Decision Jun 29, 1987
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
190
Applicant Total
111
Review Days
139

Basic Information

Device Name
NIGHTWATCH(TM) SYSTEM
K Number
K870578
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
BUCKMAN CO., INC.
Date Received
February 10, 1987
Decision Date
June 29, 1987
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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