The following data is part of a premarket notification filed by Medequip Co. with the FDA for Med-equip Corporation.
| Device ID | K915076 |
| 510k Number | K915076 |
| Device Name: | MED-EQUIP CORPORATION |
| Classification | Hearing Aid, Air Conduction |
| Applicant | MEDEQUIP CO. 1040 S.KING ST. Honolulu, HI 96814 |
| Contact | Howard K.tamashiro |
| Correspondent | Howard K.tamashiro MEDEQUIP CO. 1040 S.KING ST. Honolulu, HI 96814 |
| Product Code | ESD |
| CFR Regulation Number | 874.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-11-08 |
| Decision Date | 1992-01-09 |