AIRPURGE— 510(k) DEN080009
UnknownAnesthesia Safety Products, LLC
FDA 510(k) clearance DEN080009 for AIRPURGE, Unknown on 2014-03-04. Applicant: Anesthesia Safety Products, LLC. Device class: 2.
Clearance details
- Applicant
- Anesthesia Safety Products, LLC
- Product code
- Code OKL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5445
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Woburn, MA, US
Recent devices under product code OKL
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