The following data is part of a premarket notification filed by Cheetah Medical Inc. with the FDA for Cheetah Reliant, Cheetah Active.
| Device ID | K072662 |
| 510k Number | K072662 |
| Device Name: | CHEETAH RELIANT, CHEETAH ACTIVE |
| Classification | Plethysmograph, Impedance |
| Applicant | CHEETAH MEDICAL INC. INDUSTRIAL PARK 13 Mizpe Aviv, M.p. Misgav, IL 20187 |
| Contact | Benny Arazy |
| Correspondent | Benny Arazy CHEETAH MEDICAL INC. INDUSTRIAL PARK 13 Mizpe Aviv, M.p. Misgav, IL 20187 |
| Product Code | DSB |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-09-21 |
| Decision Date | 2008-01-16 |
| Summary: | summary |