The following data is part of a premarket notification filed by Cheetah Medical Inc. with the FDA for Cheetah Reliant.
Device ID | K103166 |
510k Number | K103166 |
Device Name: | CHEETAH RELIANT |
Classification | Plethysmograph, Impedance |
Applicant | CHEETAH MEDICAL INC. 12154 DARNESTOWN RD. #236 Gaithersburg, MD 20878 |
Contact | Rhona Shanker |
Correspondent | Rhona Shanker CHEETAH MEDICAL INC. 12154 DARNESTOWN RD. #236 Gaithersburg, MD 20878 |
Product Code | DSB |
Subsequent Product Code | DQA |
Subsequent Product Code | DXN |
CFR Regulation Number | 870.2770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-10-27 |
Decision Date | 2011-01-25 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
72900130302906 | K103166 | 000 |
07290013030030 | K103166 | 000 |
07290013030290 | K103166 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CHEETAH RELIANT 77112650 3502326 Dead/Cancelled |
CHEETAH MEDICAL, INC. 2007-02-21 |