The following data is part of a premarket notification filed by Endocare, Inc. with the FDA for Endocre Cryocare Cryosurgical System.
| Device ID | K980110 |
| 510k Number | K980110 |
| Device Name: | ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM |
| Classification | Unit, Cryosurgical, Accessories |
| Applicant | ENDOCARE, INC. 7 STUDEBAKER Irvine, CA 92618 |
| Contact | Vin Cutarelli |
| Correspondent | Vin Cutarelli ENDOCARE, INC. 7 STUDEBAKER Irvine, CA 92618 |
| Product Code | GEH |
| CFR Regulation Number | 878.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-01-12 |
| Decision Date | 1998-04-10 |
| Summary: | summary |