Dignitana AB DigniCap System— 510(k) DEN150010

Unknown

Dignitana AB

FDA 510(k) clearance DEN150010 for Dignitana AB DigniCap System, Unknown on 2015-12-08. Applicant: Dignitana AB. Device class: 2.

Clearance details

Applicant: Dignitana AB
Product code: Code PMC
Device class: Class 2
Regulation: 21 CFR 878.4360
Advisory panel: General, Plastic Surgery
Date received: 2015-03-06
Decision date: 2015-12-08
Decision: Unknown
Clearance type: Direct
Location: Lund, SE

View on FDA.gov ↗

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