The following data is part of a premarket notification filed by Ad-tech Medical Instrument Corp. with the FDA for Wyler Sphenoidal Electrode.
| Device ID | K861031 |
| 510k Number | K861031 |
| Device Name: | WYLER SPHENOIDAL ELECTRODE |
| Classification | Electrode, Depth |
| Applicant | AD-TECH MEDICAL INSTRUMENT CORP. 1901 WILLIAM ST. Racine, WI 53404 -1876 |
| Contact | David Putz |
| Correspondent | David Putz AD-TECH MEDICAL INSTRUMENT CORP. 1901 WILLIAM ST. Racine, WI 53404 -1876 |
| Product Code | GZL |
| CFR Regulation Number | 882.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-03-18 |
| Decision Date | 1986-08-25 |