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FDA 510(k)

LIFE WATCH RESPIRATORY MONITOR

K-Number: K853840 · 1985-12-09

ApplicantThe Perkin-Elmer Corp.
Decision Date1985-12-09
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIFE WATCH RESPIRATORY MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1985-12-09 under 510(k) number K853840. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE WATCH RESPIRATORY MONITOR?

LIFE WATCH RESPIRATORY MONITOR is a medical device that received FDA 510(k) clearance on 1985-12-09. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K853840.

When did LIFE WATCH RESPIRATORY MONITOR receive FDA 510(k) clearance?

LIFE WATCH RESPIRATORY MONITOR received FDA 510(k) clearance on 1985-12-09, under 510(k) number K853840.

Who is the listed applicant for LIFE WATCH RESPIRATORY MONITOR?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFE WATCH RESPIRATORY MONITOR?

The FDA product code for LIFE WATCH RESPIRATORY MONITOR is CHL.

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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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