Endocare, Inc.
FDA 510(k) & PMA Approved Devices — 22 products
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Total Devices22
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K101333 | CRYOCARE CS SURGICAL SYSTEM | GEH | 2010-06-14 | View |
| 510(k) | K062175 | CRYOCARE CN2 SYSTEM | GEH | 2006-08-28 | View |
| 510(k) | K060279 | CRYOCARE CS SURGICAL SYSTEM | GEH | 2006-02-28 | View |
| 510(k) | K050347 | MODIFICATION TO CRYOCARE CS SURGICAL SYSTEM | GEH | 2005-02-25 | View |
| 510(k) | K032333 | CRYOCARE CS SURGICAL SYSTEM | GEH | 2003-08-12 | View |
| 510(k) | K023757 | CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20 | GEH | 2002-12-05 | View |
| 510(k) | K021010 | MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE | OCL | 2002-06-06 | View |
| 510(k) | K020082 | ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM | LKY | 2002-02-05 | View |
| 510(k) | K011074 | CRYOCARE SURGICAL SYSTEM | GEH | 2002-01-25 | View |
| 510(k) | K003811 | CRYOCARE SURGICAL SYSTEM | GEH | 2001-10-11 | View |
| 510(k) | K011040 | CRYOCARE CARDIAC SURGICAL SYSTEM | OCL | 2001-06-15 | View |
| 510(k) | K003528 | SANARUS CORE TISSUE BIOPSY SYSTEM | KNW | 2001-05-03 | View |
| 510(k) | K010339 | ENDOCARE PERCUTANEOUS ACCESS SET | KOD | 2001-03-07 | View |
| 510(k) | K002615 | SURGICAL SYSTEM WITH CRYOGUIDE | GEH | 2000-11-13 | View |
| 510(k) | K002396 | ENDOCARE PERCUTANEOUS ACCESS SET | KOD | 2000-10-13 | View |
| 510(k) | K980110 | ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM | GEH | 1998-04-10 | View |
| 510(k) | K973686 | ENDOCARE CRYOCARE CRYOSURGICAL SYSTEM | GEH | 1997-12-22 | View |
| 510(k) | K963970 | ENDOCARE CRYOCARE CRYOSURGICAL SYSTEM URETHRAL WARMING SYSTEM | GEH | 1997-02-25 | View |
| 510(k) | K965243 | ENDOCARE ELECTROSURGICAL ELECTRODE | GEI | 1997-02-25 | View |
| 510(k) | K965118 | ENDOCARE MONOPOLAR ELECTRODE | FAS | 1997-02-25 | View |
No matching devices.
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