PULMOLIFE— 510(k) K061283

Substantially Equivalent

Micro Medical, Ltd.

FDA 510(k) clearance K061283 for PULMOLIFE, Substantially Equivalent on 2006-12-14. Applicant: Micro Medical, Ltd.. Device class: 2.

Clearance details

Applicant: Micro Medical, Ltd.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 2006-05-08
Decision date: 2006-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatham, Kent, 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.