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 |