PRESET FLOWMETER— 510(k) K812419

Substantially Equivalent

Timeter Instrument Corp.

FDA 510(k) clearance K812419 for PRESET FLOWMETER, Substantially Equivalent on 1981-09-21. Applicant: Timeter Instrument Corp..

Clearance details

Applicant: Timeter Instrument Corp.
Product code: Code CAX
Advisory panel: Anesthesiology
Date received: 1981-08-24
Decision date: 1981-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code CAX

product code CAX

Death: 3
Other: 1
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.