Kretztechnik AG
Solon, OH, US
Kretztechnik AG appears in FDA device records in Solon, OH. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Kretztechnik AG between 1990 and 1993. The busiest year on record is 1990, with 2. The most recent is 1993, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 2 |
| 1991 | 1 |
| 1992 | 2 |
| 1993 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K925354 | COMBISON(R) 311 | IYO | Substantially Equivalent | |
| K904070 | COMBISON(R) 330, MODEL # IR17.5AG/A & VRW177AK/A | IYO | Substantially Equivalent | |
| K910966 | SECTOR TRANSDUCER MODEL NO. AWP3.5/A | ITX | Substantially Equivalent | |
| K904665 | MODEL IW17.5A INTRA OPERATIVE TRANSDUCER | ITX | Substantially Equivalent | |
| K901725 | ADD'L TRANSDUCER FOR USE W/THE COMBISON 310A | ITX | Substantially Equivalent | |
| K901655 | 1 TRANSDUCER FOR COMBISON 310A | ITX | 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