REGULATOR, OXYGEN MECHANICAL— 510(k) K803207

Name: FDA 510(k) clearance K803207
Creator: U.S. Food and Drug Administration
Published: 1981-01-15

Substantially Equivalent

Timeter Instrument Corp.

FDA 510(k) clearance K803207 for REGULATOR, OXYGEN MECHANICAL, Substantially Equivalent on 1981-01-15. Applicant: Timeter Instrument Corp.. Device class: 1.

Clearance details

Applicant: Timeter Instrument Corp.
Product code: Code CAN
Device class: Class 1
Regulation: 21 CFR 868.2700
Advisory panel: Anesthesiology
Date received: 1980-12-18
Decision date: 1981-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K061785 — CYL-FIL OXYGEN SYSTEM2006-09-07
K950777 — OXYGEN REGULATOR1995-04-14

More clearances from Timeter Instrument Corp.

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K875075 — RT-200 COMPUTER INTERFACE1988-04-21
K875074 — VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM20001988-02-22
K871603 — CRITERION II & IIA OXYGEN CONCENTRATORS1987-08-13
K864836 — L.A.P. SPIROMETER1987-03-06
K834274 — CRITERION I1984-04-13

Adverse events under product code CAN

product code CAN

Death: 4
Other: 1
Total: 5

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.