The following data is part of a premarket notification filed by Mettler Electronics Corp. with the FDA for Midification Sys*stim 207 (model-me207).
Device ID | K855249 |
510k Number | K855249 |
Device Name: | MIDIFICATION SYS*STIM 207 (MODEL-ME207) |
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 | 1985-12-26 |
Decision Date | 1986-03-28 |