The following data is part of a premarket notification filed by Cogan Corp. with the FDA for Cogan Corp Kits Of Dental Hand Instruments.
| Device ID | K915299 |
| 510k Number | K915299 |
| Device Name: | COGAN CORP KITS OF DENTAL HAND INSTRUMENTS |
| Classification | Attachment, Precision, All |
| Applicant | COGAN CORP. 2891 N.W. ARIEL TERRACE Portland, OR 97210 |
| Contact | Gerald L Cogan |
| Correspondent | Gerald L Cogan COGAN CORP. 2891 N.W. ARIEL TERRACE Portland, OR 97210 |
| Product Code | EGG |
| CFR Regulation Number | 872.3165 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-19 |
| Decision Date | 1992-01-31 |