Tri-Tech, Inc.
Mchenry, IL, US
Tri-Tech, Inc. appears in FDA device records in Mchenry, IL. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Tri-Tech, Inc. between 1981 and 1997. The busiest year on record is 1991, with 4. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 1 |
| 1985 | 1 |
| 1990 | 1 |
| 1991 | 4 |
| 1993 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K971111 | TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER | JKA | Substantially Equivalent | |
| K952246 | TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT | JXA | Substantially Equivalent | |
| K922343 | TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT | JKA | Unknown | |
| K922342 | TRI-TECH INC. CUSTOM BLOOD ALCOHOL | JKA | Unknown | |
| K912140 | STAIRMASTER MODEL 6000 ERGOMETER | ISD | Substantially Equivalent | |
| K912058 | GAUNTLET STAIR CLIMBER | ISD | Substantially Equivalent | |
| K912057 | 4000 PT EXERCISE SYSTEM | ISD | Substantially Equivalent | |
| K912056 | GRAVITRON UPPER BODY SYSTEM EXERCISER | ISD | Substantially Equivalent | |
| K900983 | TRI-TECH URINE SPECIMEN KIT | FMH | Substantially Equivalent | |
| K843839 | STAT/PB REAGENT | DOF | Substantially Equivalent | |
| K813075 | TRITEC DOC TM | BZD | 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