The following data is part of a premarket notification filed by Baker Instructions Corp. with the FDA for System 9000 Automated Cell Counter.
Device ID | K870603 |
510k Number | K870603 |
Device Name: | SYSTEM 9000 AUTOMATED CELL COUNTER |
Classification | Counter, Cell, Automated (particle Counter) |
Applicant | BAKER INSTRUCTIONS CORP. 3085 SHAWNEE DR. P.O. BOX 2867 Winchester, VA 22601 |
Contact | R. E Tomalesky |
Correspondent | R. E Tomalesky BAKER INSTRUCTIONS CORP. 3085 SHAWNEE DR. P.O. BOX 2867 Winchester, VA 22601 |
Product Code | GKL |
CFR Regulation Number | 864.5200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-02-11 |
Decision Date | 1987-03-31 |