The following data is part of a premarket notification filed by Military Engineering, Inc. with the FDA for Curette Set, Antrum, Coakley.
| Device ID | K872609 |
| 510k Number | K872609 |
| Device Name: | CURETTE SET, ANTRUM, COAKLEY |
| Classification | Curette, Nasal |
| Applicant | MILITARY ENGINEERING, INC. P.O. BOX J 2135 WESTERN AVENUE Plymouth, IN 46563 |
| Contact | Robert W Francis |
| Correspondent | Robert W Francis MILITARY ENGINEERING, INC. P.O. BOX J 2135 WESTERN AVENUE Plymouth, IN 46563 |
| Product Code | KAP |
| CFR Regulation Number | 874.4420 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-06 |
| Decision Date | 1987-07-15 |