Reznik Instruments
Reznik Instruments appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Oct 26, 1981.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K812205 | FORCEP | Oct 26, 1981 |
| K812201 | PHOTOGRAPHIC EQUIPMENT | Oct 19, 1981 |
| K812199 | TROCAR & TROCAR SLEEVES | Oct 13, 1981 |
| K812206 | LAPAROSCOPE | Oct 13, 1981 |
| K812204 | UTERINE MANIPULATORS | Oct 13, 1981 |
| K812203 | ELECTROSURGICAL UNIT | Oct 13, 1981 |
| K812200 | INSUFFLATOR | Sep 29, 1981 |
| K812202 | FIBER OPTIC LIGHT SOURCE | Sep 29, 1981 |
| K812198 | ACCESSORIES(PROBES, SUCTION TUBES, ETC.) | Sep 11, 1981 |