RESPIRATION MONITOR— 510(k) K832999

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K832999 for RESPIRATION MONITOR, Substantially Equivalent on 1984-02-13. Applicant: Litton Medical Electronics. Device class: 2.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code FLS
Device class: Class 2
Regulation: 21 CFR 868.2377
Advisory panel: Anesthesiology
Date received: 1983-08-18
Decision date: 1984-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.