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FDA 510(k)

FR6000 FLOWMETER

K-Number: K884973 · 1989-01-17

ApplicantKey Instruments
Decision Date1989-01-17
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FR6000 FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Key Instruments. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K884973. 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 FR6000 FLOWMETER?

FR6000 FLOWMETER is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Key Instruments. The 510(k) number is K884973.

When did FR6000 FLOWMETER receive FDA 510(k) clearance?

FR6000 FLOWMETER received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884973.

Who is the listed applicant for FR6000 FLOWMETER?

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

What is the FDA product code for FR6000 FLOWMETER?

The FDA product code for FR6000 FLOWMETER is CAX.

Related Clinical Trials

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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 MedicalK872718SERIES D FLOWMETERPuritan Bennett Corp.K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter GroupK862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.K854067SELECT FLOWMETERPrecision Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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