TYPE 9240 ECG/RESP SYST ATHENA (ADULT & PEDIATIC)— 510(k) K884120

Name: FDA 510(k) clearance K884120
Creator: U.S. Food and Drug Administration
Published: 1990-07-17

Substantially Equivalent

S & W Medico Teknik

FDA 510(k) clearance K884120 for TYPE 9240 ECG/RESP SYST ATHENA (ADULT & PEDIATIC), Substantially Equivalent on 1990-07-17. Applicant: S & W Medico Teknik. Device class: 2.

Clearance details

Applicant: S & W Medico Teknik
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1988-09-30
Decision date: 1990-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denmark, DK

Download summary PDF View on FDA.gov ↗

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