The following data is part of a premarket notification filed by Radiant Medical with the FDA for Reprieve Endovascular Temperature Therapy System.
Device ID | K071358 |
510k Number | K071358 |
Device Name: | REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM |
Classification | System, Hypothermia, Intravenous, Cooling |
Applicant | RADIANT MEDICAL 250 CHESAPEAKE DR. Redwood City, CA 94063 |
Contact | Scott A Wilson |
Correspondent | Scott A Wilson RADIANT MEDICAL 250 CHESAPEAKE DR. Redwood City, CA 94063 |
Product Code | NCX |
CFR Regulation Number | 870.5900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-05-15 |
Decision Date | 2007-06-01 |
Summary: | summary |