The following data is part of a premarket notification filed by Csa Medical, Inc. with the FDA for Cryospray Ablation System, Model Cc2-nam.
Device ID | K072651 |
510k Number | K072651 |
Device Name: | CRYOSPRAY ABLATION SYSTEM, MODEL CC2-NAM |
Classification | Unit, Cryosurgical, Accessories |
Applicant | CSA MEDICAL, INC. 1101 E. 33RD STREET THIRD FLOOR - #E305 Baltimore, MD 21218 |
Contact | Jennifer Cartledge |
Correspondent | Jennifer Cartledge CSA MEDICAL, INC. 1101 E. 33RD STREET THIRD FLOOR - #E305 Baltimore, MD 21218 |
Product Code | GEH |
CFR Regulation Number | 878.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-09-19 |
Decision Date | 2007-12-07 |
Summary: | summary |