The following data is part of a premarket notification filed by Cheetah Medical Inc. with the FDA for Cheetah I.v.d.s., Model 2002p.
| Device ID | K023370 |
| 510k Number | K023370 |
| Device Name: | CHEETAH I.V.D.S., MODEL 2002P |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | CHEETAH MEDICAL INC. 117 AHUZAH ST. Ra'ananna, IL 43373 |
| Contact | Arava Hacohen |
| Correspondent | Arava Hacohen CHEETAH MEDICAL INC. 117 AHUZAH ST. Ra'ananna, IL 43373 |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-10-08 |
| Decision Date | 2002-12-24 |
| Summary: | summary |