The following data is part of a premarket notification filed by Keithley Instruments, Inc. with the FDA for Keithley Model 75100 & 75200.
| Device ID | K854110 |
| 510k Number | K854110 |
| Device Name: | KEITHLEY MODEL 75100 & 75200 |
| Classification | System, X-ray, Stationary |
| Applicant | KEITHLEY INSTRUMENTS, INC. 2875 AURORA RD. Cleveland, OH 44139 |
| Contact | Jerry L Nickol |
| Correspondent | Jerry L Nickol KEITHLEY INSTRUMENTS, INC. 2875 AURORA RD. Cleveland, OH 44139 |
| Product Code | KPR |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-10-08 |
| Decision Date | 1986-03-06 |