Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE

K-Number: K945931 · 1995-03-03

ApplicantResearch Industries Corp.
Decision Date1995-03-03
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Research Industries Corp.. It received FDA 510(k) clearance on 1995-03-03 under 510(k) number K945931. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE?

RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE is a medical device that received FDA 510(k) clearance on 1995-03-03. The listed applicant is Research Industries Corp.. The 510(k) number is K945931.

When did RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE receive FDA 510(k) clearance?

RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE received FDA 510(k) clearance on 1995-03-03, under 510(k) number K945931.

Who is the listed applicant for RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE?

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

What is the FDA product code for RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE?

The FDA product code for RMI CIRKUIT-GUARD(TM) PRESSURE RELIEF VALVE is DTL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Research Industries 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.

K833433PHYSIO-PROBE-HIGH PERMEABILITY CATH.K832542I.V. ADMINISTRATION SETK831769VARIOUS CARDIOVASCULAR SURGICAL DEVICEK831759INTRACARDIA SUCKERS

Related Devices (Code: DTL)

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.

K131124COLIGNJilin Coronado Medical , Ltd.K123448AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH BALANCE BIOSURFACE, AFFINITY FLEXIBLE LUER LOCK ADAPTER WITH CARMEDA BIOACTIVEMedtronic, Inc.K122811CONNECTOR COMPONENTS WITH BALANCE BIOSURFACEMedtronic, Inc.K122301GUARDIAN II HEMOSTASIS VALVE GUARDIAN II NC HEMOSTASIS VALVEVascular Solutions Zerusa , Ltd.K120069MEDLINE STOPCOCK AND MANIFOLDMedline Industries, Inc.K113148E-PASSSynexmed(Shenzhen)Company Limited

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.

↑