Tti Medical
Lafayette, CA, US
Tti Medical appears in FDA device records in Lafayette, CA. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Tti Medical between 1987 and 1995. The busiest year on record is 1995, with 3. The most recent is 1995, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 2 |
| 1989 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1993 | 1 |
| 1995 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K952006 | ACCU-BEAM FIBER OPTIC HANDPIECE | GEX | Substantially Equivalent | |
| K951895 | ACCU-BEAM 300W XENON LIGHT SOURCE | GCT | Substantially Equivalent | |
| K945648 | ACCU-BEAM C02 LASER HANDPIECE | GEX | Substantially Equivalent | |
| K921208 | ACCU-BEAM TUBE SET | GCJ | Substantially Equivalent | |
| K910978 | ACCU-BEAM LAPAROSCOPIC SYSTEM | GEI | Substantially Equivalent | |
| K895656 | ACCU-BEAM WAVEGUIDE | GEX | Substantially Equivalent | |
| K890922 | ACCU-BEAM YAG FIBER | GEX | Substantially Equivalent | |
| K870063 | CO2 LASER BRONCHOSCOPE SET | EOQ | Substantially Equivalent | |
| K870046 | DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET | HHR | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain