The following data is part of a premarket notification filed by Instrument Makar, Inc. with the FDA for I.m. Arthroscope.
| Device ID | K821847 |
| 510k Number | K821847 |
| Device Name: | I.M. ARTHROSCOPE |
| Classification | Arthroscope |
| Applicant | INSTRUMENT MAKAR, INC. 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 | 1982-06-22 |
| Decision Date | 1982-07-22 |