BIOLUCENT APPLICATOR KIT— 510(k) K070659

Unknown

Biolucent, Inc.

FDA 510(k) clearance K070659 for BIOLUCENT APPLICATOR KIT, Unknown on 2007-04-04. Applicant: Biolucent, Inc.. Device class: 2.

Clearance details

Applicant: Biolucent, Inc.
Product code: Code JAQ
Device class: Class 2
Regulation: 21 CFR 892.5700
Advisory panel: Radiology
Date received: 2007-03-09
Decision date: 2007-04-04
Decision: Unknown
Clearance type: Special
Location: Aliso Viejo, CA, US

Download summary PDF View on FDA.gov ↗

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