FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

2-CHANNEL RECORDER

K Number: K832998 · Decision Jun 1, 1984
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
38
Review Days
288

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Basic Information

Device Name
2-CHANNEL RECORDER
K Number
K832998
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.2810
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Litton Medical Electronics
Date Received
August 18, 1983
Decision Date
June 1, 1984
Product Code
DSF
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
DSF Recorder, Paper Chart

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Other Clearances by Litton Medical Electronics

K Number Device Name
K840522 RECOMED BLOOD-FLOW METER H236-052-02
K840899 SERVOMED ARRHYCOMP CENTRAL MONITOR SYS
K840439 RECOMED CARDIAC OUTPUT METER 236067-
K840523 SERVOMED PULSE AMPLIFIER MODULE-206-
K840524 SERVOMED BASIC BEDSIDE UNIT SMV 110TP
K840209 SERVOMED MEDIVISION SCOPE SMV-235
K840832 SERVOMED OXCARDIORE SPIROGRAPH 324/111
K840521 SERVOMED DIGITAL DISPLAY MODULE
K832250 SERVOMED BASIC BEDSIDE UNIT SMA 102-
K834600 RECOMB ECG PREAMPLIFIER/206 069 03
Search all 38 clearances from Litton Medical Electronics →