Endoscopic Technologies, Inc.
Alameda, CA, US
Endoscopic Technologies, Inc. appears in FDA device records in Alameda, CA. FDA records list 8 510(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
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Endoscopic Technologies, Inc. between 1993 and 2006. The busiest year on record is 1994, with 2. The most recent is 2006, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 1 |
| 1994 | 2 |
| 1995 | 2 |
| 2005 | 1 |
| 2006 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K060101 | ESTECH AORTIC EASY FLOW CANNULA | DWF | Substantially Equivalent | |
| K053326 | ESTECH COBRA ELECTROSURGICAL UNIT & CABLE | GEI | Substantially Equivalent | |
| K053100 | ESTECH COBRA BIPOLAR SYSTEM | GEI | Substantially Equivalent | |
| K946105 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES | GEI | Substantially Equivalent | |
| K945978 | TUBING, NONINVASIVE | GAZ | Substantially Equivalent | |
| K945979 | TROCAR/CANNULA | GCJ | Substantially Equivalent | |
| K924057 | DISPOSIBLE ELECTRO COAGULATION PROBE | GEI | Substantially Equivalent | |
| K922685 | TROCARS | GCJ | 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