The following data is part of a premarket notification filed by Cheetah Medical Inc. with the FDA for Cheetah Reliant.
| Device ID | K083093 |
| 510k Number | K083093 |
| 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 |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-10-17 |
| Decision Date | 2008-12-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07290013030030 | K083093 | 000 |
| 07290013030269 | K083093 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CHEETAH RELIANT 77112650 3502326 Dead/Cancelled |
CHEETAH MEDICAL, INC. 2007-02-21 |