Company ยท US
Telos Medical Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1992. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 27, 1992 | K920375 | DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER Telos Medical Corp. | HFN |
| Apr 3, 1992 | K920044 | DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT Telos Medical Corp. | KXO |
| Dec 30, 1991 | K914387 | TRANSCERVICAL INTRAUTERINE KIT Telos Medical Corp. | HGS |
| Jan 16, 1991 | K905018 | LAB-SITE SAFETY NEEDLE Telos Medical Corp. | DQO |
| Jan 15, 1991 | K905017 | LAB-SITE Telos Medical Corp. | DQO |
| Oct 12, 1989 | K882224 | ULTRANS DISPOSABLE INTRAUTERINE Telos Medical Corp. | HFN |
| Dec 13, 1988 | K883832 | CATHETER, INTRAUTERINE AND INTRODUCER Telos Medical Corp. | KXO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||