I-Rep, Inc.
I-Rep, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 2, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K930692 | LATHAM TABLE | February 2, 1994 |
| K930691 | ACCUTRAC TRACTION UNIT | July 22, 1993 |
| K861864 | MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT | July 14, 1986 |
| K854947 | REHABILITATION TABLES | January 3, 1986 |
| K851690 | ADJUSTABLE TREATMENT TABLES | May 7, 1985 |
| K842268 | VACUPULSE VACUUM UNIT | July 20, 1984 |
| K832940 | ROTAGYM | November 7, 1983 |
| K822906 | PHYSICAL MEDICINE & REHABILITATION EQUIP | October 15, 1982 |