WALLABY(TM) BLANKET— 510(k) K883779
Substantially EquivalentFiberoptic Medical Products, Inc.
FDA 510(k) clearance K883779 for WALLABY(TM) BLANKET, Substantially Equivalent on 1988-11-14. Applicant: Fiberoptic Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Fiberoptic Medical Products, Inc.
- Product code
- Code LBI
- Device class
- Class 2
- Regulation
- 21 CFR 880.5700
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Philadelphia, PA, US
Recent devices under product code LBI
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