VRLXP, MODEL XP— 510(k) K091732
Substantially EquivalentDeep Breeze , Ltd.
FDA 510(k) clearance K091732 for VRLXP, MODEL XP, Substantially Equivalent on 2010-03-04. Applicant: Deep Breeze , Ltd.. Device class: 2.
Clearance details
- Applicant
- Deep Breeze , Ltd.
- Product code
- Code OCR
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code OCR
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