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FDA 510(k)

LUNG VOLUME & PRESSURE MONITOR

K-Number: K771407 · 1977-08-04

ApplicantResearch Development Corp.
Decision Date1977-08-04
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LUNG VOLUME & PRESSURE 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 1977-08-04 under 510(k) number K771407. 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 VOLUME & PRESSURE MONITOR?

LUNG VOLUME & PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Research Development Corp.. The 510(k) number is K771407.

When did LUNG VOLUME & PRESSURE MONITOR receive FDA 510(k) clearance?

LUNG VOLUME & PRESSURE MONITOR received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771407.

Who is the listed applicant for LUNG VOLUME & PRESSURE 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 VOLUME & PRESSURE MONITOR?

The FDA product code for LUNG VOLUME & PRESSURE MONITOR is BZQ.

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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 PNEUMOTK771019LUNG-MECHANICS MONITORK770785MONITOR, RESPIRATORY, TWO-GAS, RDCK770061VO RESPIRATORY PNEUMOTACHOGRAPH

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Official Source

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