The following data is part of a premarket notification filed by Edward Weck, Inc. with the FDA for Visistat Skin Stapling Device.
| Device ID | K844837 |
| 510k Number | K844837 |
| Device Name: | VISISTAT SKIN STAPLING DEVICE |
| Classification | Staple, Removable (skin) |
| Applicant | EDWARD WECK, INC. P.O. BOX 12600 WECK DRIVE Research Triangle Pa, NC 27709 |
| Contact | Jeffrey Green |
| Correspondent | Jeffrey Green EDWARD WECK, INC. P.O. BOX 12600 WECK DRIVE Research Triangle Pa, NC 27709 |
| Product Code | GDT |
| CFR Regulation Number | 878.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-12-12 |
| Decision Date | 1985-01-23 |