The following data is part of a premarket notification filed by Cp Bio-medical Corp. with the FDA for Patpos Red.
| Device ID | K930296 |
| 510k Number | K930296 |
| Device Name: | PATPOS RED |
| Classification | Monitor, Patient Position, Light-beam |
| Applicant | CP BIO-MEDICAL CORP. 153 E.PALMETTO PARK RD. SUITE 133 Boca Raton, FL 33432 |
| Contact | Van Arkel |
| Correspondent | Van Arkel CP BIO-MEDICAL CORP. 153 E.PALMETTO PARK RD. SUITE 133 Boca Raton, FL 33432 |
| Product Code | IWE |
| CFR Regulation Number | 892.5780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-21 |
| Decision Date | 1993-05-21 |