VERIMED MYO/PREMS— 510(k) K874212
Substantially EquivalentVerimed Holdings, Inc.
FDA 510(k) clearance K874212 for VERIMED MYO/PREMS, Substantially Equivalent on 1988-08-08. Applicant: Verimed Holdings, Inc.. Device class: 2.
Clearance details
- Applicant
- Verimed Holdings, Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fort Lauderdale, FL, US
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