VERIMED MYOEXORCISER III (MYO III)— 510(k) K892649
Substantially EquivalentVerimed Holdings, Inc.
FDA 510(k) clearance K892649 for VERIMED MYOEXORCISER III (MYO III), Substantially Equivalent on 1989-12-13. Applicant: Verimed Holdings, Inc.. Device class: 2.
Clearance details
- Applicant
- Verimed Holdings, Inc.
- Product code
- Code HCC
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fort Lauderdale, FL, US
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