VERIMED MYOEXORCISER VERISTIM— 510(k) K893220
Substantially EquivalentVerimed Holdings, Inc.
FDA 510(k) clearance K893220 for VERIMED MYOEXORCISER VERISTIM, Substantially Equivalent on 1990-03-07. 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
Recent devices under product code IPF
view allMore clearances from Verimed Holdings, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.