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)

MODEL 54 FLOWMETER BACK-PRESSURE TUBE

K-Number: K791648 · 1979-09-17

ApplicantHarris Calorific
Decision Date1979-09-17
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 54 FLOWMETER BACK-PRESSURE TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Harris Calorific. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791648. 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 MODEL 54 FLOWMETER BACK-PRESSURE TUBE?

MODEL 54 FLOWMETER BACK-PRESSURE TUBE is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Harris Calorific. The 510(k) number is K791648.

When did MODEL 54 FLOWMETER BACK-PRESSURE TUBE receive FDA 510(k) clearance?

MODEL 54 FLOWMETER BACK-PRESSURE TUBE received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791648.

Who is the listed applicant for MODEL 54 FLOWMETER BACK-PRESSURE TUBE?

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

What is the FDA product code for MODEL 54 FLOWMETER BACK-PRESSURE TUBE?

The FDA product code for MODEL 54 FLOWMETER BACK-PRESSURE TUBE 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 Harris Calorific 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.

K810132MODEL 2 FLOWMETER

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.

↑