The following data is part of a premarket notification filed by Symbiosis Corp. with the FDA for Symbiosis Reusable Arthroscopic Surgical Inst..
| Device ID | K924016 |
| 510k Number | K924016 |
| Device Name: | SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. |
| Classification | Arthroscope |
| Applicant | SYMBIOSIS CORP. 8600 N.W. 41 ST. Miami, FL 33166 |
| Contact | Kevin W Smith |
| Correspondent | Kevin W Smith SYMBIOSIS CORP. 8600 N.W. 41 ST. Miami, FL 33166 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-11 |
| Decision Date | 1993-12-06 |