The following data is part of a premarket notification filed by Devon Industries, Inc. with the FDA for Protector, Surgical Instrument.
| Device ID | K760320 |
| 510k Number | K760320 |
| Device Name: | PROTECTOR, SURGICAL INSTRUMENT |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | DEVON INDUSTRIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-07-26 |
| Decision Date | 1976-09-30 |