The following data is part of a premarket notification filed by Mettler Electronics Corp. with the FDA for Sys*stim 206 (model-me 206).
| Device ID | K860107 |
| 510k Number | K860107 |
| Device Name: | SYS*STIM 206 (MODEL-ME 206) |
| Classification | Stimulator, Muscle, Powered |
| Applicant | METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. Anaheim, CA 92805 |
| Contact | Robert Fleming |
| Correspondent | Robert Fleming METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. Anaheim, CA 92805 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-01-13 |
| Decision Date | 1986-03-28 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816864020005 | K860107 | 000 |