The following data is part of a premarket notification filed by Wr Medical Electronics Co. with the FDA for Case Iv Computer Aided Sensory Evaluator Version 4.
| Device ID | K910624 |
| 510k Number | K910624 |
| Device Name: | CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 |
| Classification | Device, Vibration Threshold Measurement |
| Applicant | WR MEDICAL ELECTRONICS CO. 123 NO.2ND.STREET Stillwater, MN 55082 |
| Contact | Paul J Anderson |
| Correspondent | Paul J Anderson WR MEDICAL ELECTRONICS CO. 123 NO.2ND.STREET Stillwater, MN 55082 |
| Product Code | LLN |
| CFR Regulation Number | 882.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-12 |
| Decision Date | 1992-01-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00702173355696 | K910624 | 000 |