The following data is part of a premarket notification filed by Ge Medical Systems, Llc with the FDA for Ge Lightspeed 7.2 Ct Scanner System.
Device ID | K082761 |
510k Number | K082761 |
Device Name: | GE LIGHTSPEED 7.2 CT SCANNER SYSTEM |
Classification | System, X-ray, Tomography, Computed |
Applicant | GE MEDICAL SYSTEMS, LLC 3000 N GRANDVIEW BLVD. W-1140 Waukesha, WI 53188 |
Contact | Tracey Ortiz |
Correspondent | Jay Y Kogoma INTERTEK TESTING SERVICES 2307 EAST AURORA ROAD UNIT B7 Twinsburg, OH 44087 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2008-09-22 |
Decision Date | 2008-10-08 |
Summary: | summary |