HELIO2 BLENDER— 510(k) K090781
Substantially EquivalentPrecision Medical, Inc.
FDA 510(k) clearance K090781 for HELIO2 BLENDER, Substantially Equivalent on 2009-08-13. Applicant: Precision Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Precision Medical, Inc.
- Product code
- Code BZR
- Device class
- Class 2
- Regulation
- 21 CFR 868.5330
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Northampton, PA, US
Recent devices under product code BZR
view allMore clearances from Precision Medical, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.