ACTI-FLEX ARTERIAL EXTENSION SET— 510(k) K954035

Substantially Equivalent

R-Group Intl.

FDA 510(k) clearance K954035 for ACTI-FLEX ARTERIAL EXTENSION SET, Substantially Equivalent on 1995-09-25. Applicant: R-Group Intl.. Device class: 1.

Clearance details

Applicant: R-Group Intl.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1995-08-28
Decision date: 1995-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gainesville, FL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.