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)

FLOW LIMITER

K-Number: K791017 · 1979-07-03

ApplicantTimeter Instrument Corp.
Decision Date1979-07-03
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOW LIMITER is the device name listed in this FDA 510(k) record. The listed applicant is Timeter Instrument Corp.. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K791017. The device is classified under product code CAX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW LIMITER?

FLOW LIMITER is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K791017.

When did FLOW LIMITER receive FDA 510(k) clearance?

FLOW LIMITER received FDA 510(k) clearance on 1979-07-03, under 510(k) number K791017.

Who is the listed applicant for FLOW LIMITER?

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

What is the FDA product code for FLOW LIMITER?

The FDA product code for FLOW LIMITER is CAX.

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 Timeter Instrument 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.

K875075RT-200 COMPUTER INTERFACEK875074VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000K871603CRITERION II & IIA OXYGEN CONCENTRATORSK864836L.A.P. SPIROMETERK834274CRITERION IK823775BORDON GAGE REGULATOR #BG

View all 29 devices →

Related Devices (Code: CAX)

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.

K923781MXR-2000 FLOWMETERPorter Instrument Co., Inc.K910316OHMEDA - LOW FLOW FLOWMETEROhmeda MedicalK884973FR6000 FLOWMETERKey InstrumentsK872718SERIES D FLOWMETERPuritan Bennett Corp.K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter GroupK862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.

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.

↑