MONITOR, RESPIRATORY, TWO-GAS, RDC— 510(k) K770785

Name: FDA 510(k) clearance K770785
Creator: U.S. Food and Drug Administration
Published: 1977-05-20

Substantially Equivalent

Research Development Corp.

FDA 510(k) clearance K770785 for MONITOR, RESPIRATORY, TWO-GAS, RDC, Substantially Equivalent on 1977-05-20. Applicant: Research Development Corp.. Device class: 2.

Clearance details

Applicant: Research Development Corp.
Product code: Code KLA
Device class: Class 2
Regulation: 21 CFR 876.1725
Advisory panel: Gastroenterology, Urology
Date received: 1977-05-02
Decision date: 1977-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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