The following data is part of a premarket notification filed by John Chatillon & Sons, Inc. with the FDA for Dynamometer.
| Device ID | K964685 |
| 510k Number | K964685 |
| Device Name: | DYNAMOMETER |
| Classification | Dynamometer, Ac-powered |
| Applicant | JOHN CHATILLON & SONS, INC. 7609 BUSINESS PARK DR. Greensboro, NC 27409 -9301 |
| Contact | Joseph R Troy |
| Correspondent | Joseph R Troy JOHN CHATILLON & SONS, INC. 7609 BUSINESS PARK DR. Greensboro, NC 27409 -9301 |
| Product Code | LBB |
| CFR Regulation Number | 888.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-11-22 |
| Decision Date | 1997-01-27 |
| Summary: | summary |