Aristo Medical Products, Inc.
Aristo Medical Products, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 19, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K961060 | ARISTO ESOPHAGEAL STETHOSCOPE | June 19, 1996 |
| K960251 | COMSAT ADULT,PEDIATRIC,INFANT,NEONATAL DISPOSABLE SENSOR AND COMSAT REUSABLE FINGER SENSOR | March 26, 1996 |
| K953817 | ARISTO MEDICAL MODEL 2101 PATIENT MONITOR | November 22, 1995 |
| K920966 | SDI OXYGEN/DIGITAL OXYGEN TRANSDUCERS (DOT) | July 16, 1993 |