The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Taylor & Tycos Acoustic Sphygmomanometer.
| Device ID | K820135 |
| 510k Number | K820135 |
| Device Name: | TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-18 |
| Decision Date | 1982-03-01 |