The following data is part of a premarket notification filed by Endocare, Inc. with the FDA for Endocare Cryocare Cryosurgical System Urethral Warming System.
Device ID | K963970 |
510k Number | K963970 |
Device Name: | ENDOCARE CRYOCARE CRYOSURGICAL SYSTEM URETHRAL WARMING SYSTEM |
Classification | Unit, Cryosurgical, Accessories |
Applicant | ENDOCARE, INC. 18 TECHNOLOGY DR., SUITE 134 Irvine, CA 92718 |
Contact | Vin Cutarelli |
Correspondent | Vin Cutarelli ENDOCARE, INC. 18 TECHNOLOGY DR., SUITE 134 Irvine, CA 92718 |
Product Code | GEH |
CFR Regulation Number | 878.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-10-03 |
Decision Date | 1997-02-25 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00810563020380 | K963970 | 000 |
00810563020342 | K963970 | 000 |