I-CHANNEL RECORDER— 510(k) K833000

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K833000 for I-CHANNEL RECORDER, Substantially Equivalent on 1984-06-01. Applicant: Litton Medical Electronics. Device class: 1.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1983-08-18
Decision date: 1984-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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K902586 — GRI LASERGRAPH(TM) ECG PAPER1990-06-22
K902230 — COLORADO COLOR IMAGING RECORDER1990-06-19

More clearances from Litton Medical Electronics

K840522 — RECOMED BLOOD-FLOW METER H236-052-021985-05-16
K840439 — RECOMED CARDIAC OUTPUT METER 236067-1984-11-20
K840899 — SERVOMED ARRHYCOMP CENTRAL MONITOR SYS1984-11-20
K840523 — SERVOMED PULSE AMPLIFIER MODULE-206-1984-10-29
K840524 — SERVOMED BASIC BEDSIDE UNIT SMV 110TP1984-10-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.