The following data is part of a premarket notification filed by The Jayms Co. with the FDA for Digital Conductance Meter.
Device ID | K924313 |
510k Number | K924313 |
Device Name: | DIGITAL CONDUCTANCE METER |
Classification | Device, Biofeedback |
Applicant | THE JAYMS CO. 432 NORTH 750 EAST Lindon, UT 84042 |
Contact | Mark Galloway |
Correspondent | Mark Galloway THE JAYMS CO. 432 NORTH 750 EAST Lindon, UT 84042 |
Product Code | HCC |
CFR Regulation Number | 882.5050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-26 |
Decision Date | 1996-03-14 |
Summary: | summary |