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FDA 510(k)

RESPIRATION MONITOR

K-Number: K832999 · 1984-02-13

ApplicantLitton Medical Electronics
Decision Date1984-02-13
Product CodeFLS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1984-02-13 under 510(k) number K832999. The device is classified under product code FLS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRATION MONITOR?

RESPIRATION MONITOR is a medical device that received FDA 510(k) clearance on 1984-02-13. The listed applicant is Litton Medical Electronics. The 510(k) number is K832999.

When did RESPIRATION MONITOR receive FDA 510(k) clearance?

RESPIRATION MONITOR received FDA 510(k) clearance on 1984-02-13, under 510(k) number K832999.

Who is the listed applicant for RESPIRATION MONITOR?

The FDA 510(k) record lists Litton Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESPIRATION MONITOR?

The FDA product code for RESPIRATION MONITOR is FLS.

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Other records listing Litton Medical Electronics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K840522RECOMED BLOOD-FLOW METER H236-052-02K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840439RECOMED CARDIAC OUTPUT METER 236067-K840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840209SERVOMED MEDIVISION SCOPE SMV-235

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Related Devices (Code: FLS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K011597SMARTMONITOR 2, MODEL 4000Respironics Georgia, Inc.K991087HANNAH WIRELESS VITAL SIGNS MONITORIlife Systems, Inc.K962865REMBRANDT SYSTEMAirsep Corp.K951246PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONSProtocol Systems, Inc.K894973RESPITRACE PLUSHogan & HartsonK830778MONITORING KIT AMK-1Alternative Design Systems, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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