BORDON GAGE REGULATOR #BG— 510(k) K823775

Name: FDA 510(k) clearance K823775
Creator: U.S. Food and Drug Administration
Published: 1983-01-14

Substantially Equivalent

Timeter Instrument Corp.

FDA 510(k) clearance K823775 for BORDON GAGE REGULATOR #BG, Substantially Equivalent on 1983-01-14. Applicant: Timeter Instrument Corp.. Device class: 1.

Clearance details

Applicant: Timeter Instrument Corp.
Product code: Code CCN
Device class: Class 1
Regulation: 21 CFR 868.2300
Advisory panel: Anesthesiology
Date received: 1982-12-14
Decision date: 1983-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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