The following data is part of a premarket notification filed by Qfc Industries with the FDA for Qfc Umbilical Clamp.
| Device ID | K963889 |
| 510k Number | K963889 |
| Device Name: | QFC UMBILICAL CLAMP |
| Classification | Clamp, Umbilical |
| Applicant | QFC INDUSTRIES 2405 FOREST PARK BLVD. Fort Worth, TX 76110 -1765 |
| Contact | Glenn Crum |
| Correspondent | Glenn Crum QFC INDUSTRIES 2405 FOREST PARK BLVD. Fort Worth, TX 76110 -1765 |
| Product Code | HFW |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-09-26 |
| Decision Date | 1997-04-18 |