DISS FEMALE AIR ADAPTOR— 510(k) K813235

Name: FDA 510(k) clearance K813235
Creator: U.S. Food and Drug Administration
Published: 1981-12-08

Substantially Equivalent

Timeter Instrument Corp.

FDA 510(k) clearance K813235 for DISS FEMALE AIR ADAPTOR, Substantially Equivalent on 1981-12-08. Applicant: Timeter Instrument Corp.. Device class: 2.

Clearance details

Applicant: Timeter Instrument Corp.
Product code: Code BYK
Device class: Class 2
Regulation: 21 CFR 868.5710
Advisory panel: Anesthesiology
Date received: 1981-11-17
Decision date: 1981-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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