The following data is part of a premarket notification filed by Sentry Medical Products, Inc. with the FDA for Patient Cable.
| Device ID | K932704 |
| 510k Number | K932704 |
| Device Name: | PATIENT CABLE |
| Classification | Cable, Transducer And Electrode, Patient, (including Connector) |
| Applicant | SENTRY MEDICAL PRODUCTS, INC. 17171 MURPHY AVE. Irvine, CA 92614 -5915 |
| Contact | William E Blair |
| Correspondent | William E Blair SENTRY MEDICAL PRODUCTS, INC. 17171 MURPHY AVE. Irvine, CA 92614 -5915 |
| Product Code | DSA |
| CFR Regulation Number | 870.2900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-03 |
| Decision Date | 1993-12-27 |