Storz
St. Louis, MO, US
Storz appears in FDA device records in St. Louis, MO. 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 Storz between 1992 and 1996. The busiest year on record is 1996, with 2. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 1 |
| 1993 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960007 | STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR | MPA | Substantially Equivalent | |
| K952151 | STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204) | HQR | Substantially Equivalent | |
| K954340 | STORZ MICROFLOW PHACOEMULSIFICATION NEEDLE | HQC | Substantially Equivalent | |
| K930278 | STORZ COMPUSCAN AB | IYO | Substantially Equivalent | |
| K926512 | STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE | HQC | Substantially Equivalent | |
| K913504 | STORZ MICRO CUTTER 25 GAUGE PACK | HQE | 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