The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Microlite Microtiter Plate Luminometer Ml2250/modi.
Device ID | K915896 |
510k Number | K915896 |
Device Name: | MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly, VA 22021 |
Contact | Warren Gehle |
Correspondent | Warren Gehle DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly, VA 22021 |
Product Code | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-12-19 |
Decision Date | 1992-05-04 |