The following data is part of a premarket notification filed by Snyder Laboratories, Inc. with the FDA for Hemovac Tubing Material Change.
| Device ID | K781400 |
| 510k Number | K781400 |
| Device Name: | HEMOVAC TUBING MATERIAL CHANGE |
| Classification | Apparatus, Suction, Single Patient Use, Portable, Nonpowered |
| Applicant | SNYDER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GCY |
| CFR Regulation Number | 878.4680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-08-15 |
| Decision Date | 1978-09-20 |