PAIN BUDDY— 510(k) K102051
Substantially EquivalentBiomedical Life Systems, Inc.
FDA 510(k) clearance K102051 for PAIN BUDDY, Substantially Equivalent on 2011-07-29. Applicant: Biomedical Life Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Biomedical Life Systems, Inc.
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vista, CA, US
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