The following data is part of a premarket notification filed by Chayes Virginia, Inc. with the FDA for Perception Series Delivery Sys..
| Device ID | K771890 |
| 510k Number | K771890 |
| Device Name: | PERCEPTION SERIES DELIVERY SYS. |
| Classification | Unit, Operative Dental |
| Applicant | CHAYES VIRGINIA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EIA |
| CFR Regulation Number | 872.6640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-10-06 |
| Decision Date | 1977-10-20 |