VENTIMASK MK IV— 510(k) K951652

Substantially Equivalent

Flexicare Medical, Ltd.

FDA 510(k) clearance K951652 for VENTIMASK MK IV, Substantially Equivalent on 1995-04-27. Applicant: Flexicare Medical, Ltd.. Device class: 1.

Clearance details

Applicant: Flexicare Medical, Ltd.
Product code: Code BYF
Device class: Class 1
Regulation: 21 CFR 868.5600
Advisory panel: Anesthesiology
Date received: 1995-04-10
Decision date: 1995-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, GB

Download summary PDF View on FDA.gov ↗

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