The following data is part of a premarket notification filed by Dynatronics Laser Corp. with the FDA for Dynatron 330 Body Composition Analyzer.
Device ID | K900321 |
510k Number | K900321 |
Device Name: | DYNATRON 330 BODY COMPOSITION ANALYZER |
Classification | Plethysmograph, Impedance |
Applicant | DYNATRONICS LASER CORP. 470 LAWNDALE DRIVE, BUILDING D Salt Lake City, UT 84115 |
Contact | Cullimore, Jr |
Correspondent | Cullimore, Jr DYNATRONICS LASER CORP. 470 LAWNDALE DRIVE, BUILDING D Salt Lake City, UT 84115 |
Product Code | DSB |
CFR Regulation Number | 870.2770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-23 |
Decision Date | 1990-06-11 |