PRESET FLOWMETER
K-Number: K812419 · 1981-09-21
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Device Summary
Frequently Asked Questions
What is the PRESET FLOWMETER?
PRESET FLOWMETER is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K812419.
When did PRESET FLOWMETER receive FDA 510(k) clearance?
PRESET FLOWMETER received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812419.
Who is the listed applicant for PRESET FLOWMETER?
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 PRESET FLOWMETER?
The FDA product code for PRESET FLOWMETER 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.
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.
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.
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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