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FDA 510(k)

LUNG-MECHANICS MONITOR

K-Number: K771019 · 1977-06-14

ApplicantResearch Development Corp.
Decision Date1977-06-14
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG-MECHANICS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Research Development Corp.. It received FDA 510(k) clearance on 1977-06-14 under 510(k) number K771019. 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 LUNG-MECHANICS MONITOR?

LUNG-MECHANICS MONITOR is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Research Development Corp.. The 510(k) number is K771019.

When did LUNG-MECHANICS MONITOR receive FDA 510(k) clearance?

LUNG-MECHANICS MONITOR received FDA 510(k) clearance on 1977-06-14, under 510(k) number K771019.

Who is the listed applicant for LUNG-MECHANICS MONITOR?

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

What is the FDA product code for LUNG-MECHANICS MONITOR?

The FDA product code for LUNG-MECHANICS MONITOR is BZQ.

Related Clinical Trials

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Other records listing Research Development Corp. 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.

K871870HSC UNIT RODK791730RING-ORIFICE, TURBULENT FLOW PNEUMOTK771407LUNG VOLUME & PRESSURE MONITORK770785MONITOR, RESPIRATORY, TWO-GAS, RDCK770061VO RESPIRATORY PNEUMOTACHOGRAPH

Related Devices (Code: BZQ)

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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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