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FDA 510(k)

APNET RESPIRATION MONITOR

K-Number: K862962 · 1986-09-19

Decision Date1986-09-19
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

APNET RESPIRATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Wireless Monitors, Inc.. It received FDA 510(k) clearance on 1986-09-19 under 510(k) number K862962. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APNET RESPIRATION MONITOR?

APNET RESPIRATION MONITOR is a medical device that received FDA 510(k) clearance on 1986-09-19. The listed applicant is Wireless Monitors, Inc.. The 510(k) number is K862962.

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

APNET RESPIRATION MONITOR received FDA 510(k) clearance on 1986-09-19, under 510(k) number K862962.

Who is the listed applicant for APNET RESPIRATION MONITOR?

The FDA 510(k) record lists Wireless Monitors, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APNET RESPIRATION MONITOR?

The FDA product code for APNET RESPIRATION MONITOR is BZQ.

Related Clinical Trials

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.

Related Devices (Code: BZQ)

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.

Official Source

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