SNAP WOUND CARE DEVICE— 510(k) DEN080011

Unknown

Spiracur, Inc.

FDA 510(k) clearance DEN080011 for SNAP WOUND CARE DEVICE, Unknown on 2009-08-07. Applicant: Spiracur, Inc.. Device class: 2.

Clearance details

Applicant: Spiracur, Inc.
Product code: Code OKO
Device class: Class 2
Regulation: 21 CFR 878.4683
Advisory panel: General, Plastic Surgery
Date received: 2008-11-03
Decision date: 2009-08-07
Decision: Unknown
Clearance type: Post-NSE
Location: Philadelphia, PA, US

View on FDA.gov ↗

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