The following data is part of a premarket notification filed by Camino Laboratories, Inc. with the FDA for Model 110-5 & 140-8.
| Device ID | K842005 |
| 510k Number | K842005 |
| Device Name: | MODEL 110-5 & 140-8 |
| Classification | Transducer, Pressure, Catheter Tip |
| Applicant | CAMINO LABORATORIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DXO |
| CFR Regulation Number | 870.2870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-05-17 |
| Decision Date | 1984-08-03 |