The following data is part of a premarket notification filed by Med Labs, Inc. with the FDA for Scan Com And Scan Com P (tentative).
| Device ID | K903652 |
| 510k Number | K903652 |
| Device Name: | SCAN COM AND SCAN COM P (TENTATIVE) |
| Classification | System, Communication, Powered |
| Applicant | MED LABS, INC. 28 VEREDA CORDILLERA Goleta, CA 93117 |
| Contact | Philip D Norvell |
| Correspondent | Philip D Norvell MED LABS, INC. 28 VEREDA CORDILLERA Goleta, CA 93117 |
| Product Code | ILQ |
| CFR Regulation Number | 890.3710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-08-13 |
| Decision Date | 1990-08-24 |