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FDA 510(k)

RING-ORIFICE, TURBULENT FLOW PNEUMOT

K-Number: K791730 · 1979-11-16

ApplicantResearch Development Corp.
Decision Date1979-11-16
Product CodeJAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RING-ORIFICE, TURBULENT FLOW PNEUMOT 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 1979-11-16 under 510(k) number K791730. The device is classified under product code JAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RING-ORIFICE, TURBULENT FLOW PNEUMOT?

RING-ORIFICE, TURBULENT FLOW PNEUMOT is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Research Development Corp.. The 510(k) number is K791730.

When did RING-ORIFICE, TURBULENT FLOW PNEUMOT receive FDA 510(k) clearance?

RING-ORIFICE, TURBULENT FLOW PNEUMOT received FDA 510(k) clearance on 1979-11-16, under 510(k) number K791730.

Who is the listed applicant for RING-ORIFICE, TURBULENT FLOW PNEUMOT?

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 RING-ORIFICE, TURBULENT FLOW PNEUMOT?

The FDA product code for RING-ORIFICE, TURBULENT FLOW PNEUMOT is JAX.

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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 RODK771407LUNG VOLUME & PRESSURE MONITORK771019LUNG-MECHANICS MONITORK770785MONITOR, RESPIRATORY, TWO-GAS, RDCK770061VO RESPIRATORY PNEUMOTACHOGRAPH

Related Devices (Code: JAX)

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.

K990962FLOSENSE, MODEL 29-8010Sdi Diagnostics, Inc.K921178PTI-A, PTI-P, PTI-N DISPOSABLE PNEUMOTACHSMedical Associated Services, Inc.K884464SPIROMETRICS MODEL 2200 SM200 FLOW SENSORSpirometrics, Inc.K853085PAX METERPeace Medical, Inc.K833265RESPIRATORY FLOW MODULEThoratec Laboratories Corp.K812825FLO-COR IBiotrine Corp.

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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