Verimed Holdings, Inc.
Verimed Holdings, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 20, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K981277 | PERIFORM | November 20, 1998 |
| K954127 | BIOFEEDBACK DEVICE | November 14, 1995 |
| K951969 | MYOEXORCISER II FUAL | June 14, 1995 |
| K930670 | PHYACTION 787 | July 2, 1993 |
| K922550 | ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) | December 10, 1992 |
| K913912 | VERIMED PERINEOMETER | June 16, 1992 |
| K893220 | VERIMED MYOEXORCISER VERISTIM | March 7, 1990 |
| K892649 | VERIMED MYOEXORCISER III (MYO III) | December 13, 1989 |
| K874212 | VERIMED MYO/PREMS | August 8, 1988 |
| K854193 | ELECTRO-MYOGRAPHIC PERINEOMETER | June 9, 1986 |
| K852963 | MYO-ACTUATOR | January 21, 1986 |
| K832714 | VERIMED MYOEXORCISER | October 28, 1983 |