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FDA 510(k)

FLOWMETER, BACK PRESSURE COMPENSATED,

K-Number: K791220 · 1979-08-03

ApplicantTimeter Instrument Corp.
Decision Date1979-08-03
Product CodeCAX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOWMETER, BACK PRESSURE COMPENSATED, 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 1979-08-03 under 510(k) number K791220. 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 FLOWMETER, BACK PRESSURE COMPENSATED,?

FLOWMETER, BACK PRESSURE COMPENSATED, is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K791220.

When did FLOWMETER, BACK PRESSURE COMPENSATED, receive FDA 510(k) clearance?

FLOWMETER, BACK PRESSURE COMPENSATED, received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791220.

Who is the listed applicant for FLOWMETER, BACK PRESSURE COMPENSATED,?

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 FLOWMETER, BACK PRESSURE COMPENSATED,?

The FDA product code for FLOWMETER, BACK PRESSURE COMPENSATED, is CAX.

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Other records listing Timeter Instrument Corp. as applicant

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Related Devices (Code: CAX)

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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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