Endotherapeutics
Endotherapeutics 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 June 9, 1987.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Known Names
endo-therapeutics, endotherapeutics
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K870855 | UROSCAN | June 9, 1987 |
| K860192 | ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVE | March 17, 1986 |
| K860102 | MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE | February 12, 1986 |
| K860103 | MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE | February 12, 1986 |
| K852031 | ENDOPORT 5MM | August 13, 1985 |
| K844619 | ENDONEEDLE | January 9, 1985 |
| K841716 | ENDOPORT EROCAR | June 28, 1984 |