The following data is part of a premarket notification filed by Devon Industries, Inc. with the FDA for Devo'n Loops.
| Device ID | K830248 |
| 510k Number | K830248 |
| Device Name: | DEVO'N LOOPS |
| Classification | Instrument, Surgical, Disposable |
| Applicant | DEVON INDUSTRIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDC |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-25 |
| Decision Date | 1983-03-08 |