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FDA 510(k)

MONITOR, RESPIRATORY, TWO-GAS, RDC

K-Number: K770785 · 1977-05-20

ApplicantResearch Development Corp.
Decision Date1977-05-20
Product CodeKLA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MONITOR, RESPIRATORY, TWO-GAS, RDC 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 1977-05-20 under 510(k) number K770785. The device is classified under product code KLA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR, RESPIRATORY, TWO-GAS, RDC?

MONITOR, RESPIRATORY, TWO-GAS, RDC is a medical device that received FDA 510(k) clearance on 1977-05-20. The listed applicant is Research Development Corp.. The 510(k) number is K770785.

When did MONITOR, RESPIRATORY, TWO-GAS, RDC receive FDA 510(k) clearance?

MONITOR, RESPIRATORY, TWO-GAS, RDC received FDA 510(k) clearance on 1977-05-20, under 510(k) number K770785.

Who is the listed applicant for MONITOR, RESPIRATORY, TWO-GAS, RDC?

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 MONITOR, RESPIRATORY, TWO-GAS, RDC?

The FDA product code for MONITOR, RESPIRATORY, TWO-GAS, RDC is KLA.

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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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 MONITORK771019LUNG-MECHANICS MONITORK770061VO RESPIRATORY PNEUMOTACHOGRAPH

Related Devices (Code: KLA)

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.

K242666Fecobionics Anorectal SystemGi Bionics, LLCK242304REDNeuraxis, Inc.K234107Solar™ Anorectal Manometry Catheter (Model Number: K1210AC-L-2212)Laborie Medical Technologies, Corp.K180135THD Anopress with THD SensyProbeThd SpaK161785THD ANOPRESSThd SpaK120088MCOMPASS ANORECTAL MANOMETRY SYSTEMMedspira, LLC

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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