The following data is part of a premarket notification filed by Dynatech Laboratories, Inc. with the FDA for Microlite Camera Luminometer Cl 1050 (0119010000).
Device ID | K884782 |
510k Number | K884782 |
Device Name: | MICROLITE CAMERA LUMINOMETER CL 1050 (0119010000) |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | DYNATECH LABORATORIES, INC. 14340 SULLYFIELD CIRCLE Chantilly, VA 22021 |
Contact | Barry S Lazar |
Correspondent | Barry S Lazar 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 | 1988-11-15 |
Decision Date | 1989-02-17 |