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FDA 510(k)

BORDON GAGE REGULATOR #BG

K-Number: K823775 · 1983-01-14

ApplicantTimeter Instrument Corp.
Decision Date1983-01-14
Product CodeCCN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BORDON GAGE REGULATOR #BG 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 1983-01-14 under 510(k) number K823775. The device is classified under product code CCN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BORDON GAGE REGULATOR #BG?

BORDON GAGE REGULATOR #BG is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K823775.

When did BORDON GAGE REGULATOR #BG receive FDA 510(k) clearance?

BORDON GAGE REGULATOR #BG received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823775.

Who is the listed applicant for BORDON GAGE REGULATOR #BG?

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 BORDON GAGE REGULATOR #BG?

The FDA product code for BORDON GAGE REGULATOR #BG is CCN.

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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 IK822746RT-200 CALIBRATION ANALYZER

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Related Devices (Code: CCN)

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.

K934945FLOWMETER NIPPLE ADAPTORCardio-Search , Ltd.K920783OXYGEN FLOW CONTROLLERPuritan Bennett Corp.K872038NEB-U-VENTDesign Technologies, Inc.K871262MODIFIED NOFLO IDesign Technologies, Inc.K863613NO-FLO IDesign Technologies, Inc.K863659FLOW INTERRUPTION INDICATORSalter Labs

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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