The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Umbilical Cord Clamp.
| Device ID | K781548 |
| 510k Number | K781548 |
| Device Name: | UMBILICAL CORD CLAMP |
| Classification | Clamp, Umbilical |
| Applicant | HOLLISTER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HFW |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-09-12 |
| Decision Date | 1978-10-17 |