The following data is part of a premarket notification filed by Davis & Geck, Inc. with the FDA for Surgilon, Dermalon, & Ophthalon.
| Device ID | K981582 |
| 510k Number | K981582 |
| Device Name: | SURGILON, DERMALON, & OPHTHALON |
| Classification | Suture, Nonabsorbable, Synthetic, Polyamide |
| Applicant | DAVIS & GECK, INC. 444 MC DONNELL BLVD. Hazelwood, MO 63042 |
| Contact | Vanada Johnson |
| Correspondent | Vanada Johnson DAVIS & GECK, INC. 444 MC DONNELL BLVD. Hazelwood, MO 63042 |
| Product Code | GAR |
| CFR Regulation Number | 878.5020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-05-04 |
| Decision Date | 1998-07-13 |
| Summary: | summary |