Telos Medical Corp.
Telos Medical Corp. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 27, 1992.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K920375 | DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER | October 27, 1992 |
| K920044 | DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT | April 3, 1992 |
| K914387 | TRANSCERVICAL INTRAUTERINE KIT | December 30, 1991 |
| K905018 | LAB-SITE SAFETY NEEDLE | January 16, 1991 |
| K905017 | LAB-SITE | January 15, 1991 |
| K882224 | ULTRANS DISPOSABLE INTRAUTERINE | October 12, 1989 |
| K883832 | CATHETER, INTRAUTERINE AND INTRODUCER | December 13, 1988 |