The following data is part of a premarket notification filed by Edward Weck, Inc. with the FDA for Reynolds Double Hemoclip Appliers.
| Device ID | K790990 |
| 510k Number | K790990 |
| Device Name: | REYNOLDS DOUBLE HEMOCLIP APPLIERS |
| Classification | Applier, Surgical, Clip |
| Applicant | EDWARD WECK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GDO |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-05-30 |
| Decision Date | 1979-06-05 |