MICROTRAPPER/MICRODIGITRAPPER, MODIFICATION— 510(k) K905520

Name: FDA 510(k) clearance K905520
Creator: U.S. Food and Drug Administration
Published: 1991-04-26

Substantially Equivalent

Synectics-Dantec

FDA 510(k) clearance K905520 for MICROTRAPPER/MICRODIGITRAPPER, MODIFICATION, Substantially Equivalent on 1991-04-26. Applicant: Synectics-Dantec. Device class: 2.

Clearance details

Applicant: Synectics-Dantec
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1990-12-07
Decision date: 1991-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, US

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