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FDA 510(k)

BLSI VENTILATION MONITOR

K-Number: K810547 · 1981-03-11

ApplicantBunnell Life Systems, Inc.
Decision Date1981-03-11
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLSI VENTILATION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Bunnell Life Systems, Inc.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810547. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLSI VENTILATION MONITOR?

BLSI VENTILATION MONITOR is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Bunnell Life Systems, Inc.. The 510(k) number is K810547.

When did BLSI VENTILATION MONITOR receive FDA 510(k) clearance?

BLSI VENTILATION MONITOR received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810547.

Who is the listed applicant for BLSI VENTILATION MONITOR?

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

What is the FDA product code for BLSI VENTILATION MONITOR?

The FDA product code for BLSI VENTILATION MONITOR is CAP.

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.

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Related Devices (Code: CAP)

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.

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Official Source

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

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