The following data is part of a premarket notification filed by Cabot Medical Corp. with the FDA for Anthroscopy System.
| Device ID | K834146 |
| 510k Number | K834146 |
| Device Name: | ANTHROSCOPY SYSTEM |
| Classification | Arthroscope |
| Applicant | CABOT MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-01 |
| Decision Date | 1984-03-08 |