Company ยท US
Endotherapeutics
FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1987. 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 |
|---|---|---|---|
| Jun 9, 1987 | K870855 | UROSCAN Endotherapeutics | FAP |
| Mar 17, 1986 | K860192 | ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVE Endotherapeutics | HET |
| Feb 12, 1986 | K860103 | MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE Endotherapeutics | GCP |
| Feb 12, 1986 | K860102 | MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE Endotherapeutics | FHP |
| Aug 13, 1985 | K852031 | ENDOPORT 5MM Endotherapeutics | HET |
| Jan 9, 1985 | K844619 | ENDONEEDLE Endotherapeutics | FHO |
| Jun 28, 1984 | K841716 | ENDOPORT EROCAR Endotherapeutics | FBQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||