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FDA 510(k)

PRESSURE, LOW/HIGH MODEL C1070

K-Number: K781697 · 1978-10-27

ApplicantTimeter Instrument Corp.
Decision Date1978-10-27
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRESSURE, LOW/HIGH MODEL C1070 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 1978-10-27 under 510(k) number K781697. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURE, LOW/HIGH MODEL C1070?

PRESSURE, LOW/HIGH MODEL C1070 is a medical device that received FDA 510(k) clearance on 1978-10-27. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K781697.

When did PRESSURE, LOW/HIGH MODEL C1070 receive FDA 510(k) clearance?

PRESSURE, LOW/HIGH MODEL C1070 received FDA 510(k) clearance on 1978-10-27, under 510(k) number K781697.

Who is the listed applicant for PRESSURE, LOW/HIGH MODEL C1070?

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 PRESSURE, LOW/HIGH MODEL C1070?

The FDA product code for PRESSURE, LOW/HIGH MODEL C1070 is CAP.

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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 IK823775BORDON GAGE REGULATOR #BG

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Related Devices (Code: CAP)

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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed Corp.

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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