The following data is part of a premarket notification filed by Bio-tek Instruments, Inc. with the FDA for Ceres 900c & Ceres Uv900c.
Device ID | K942923 |
510k Number | K942923 |
Device Name: | CERES 900C & CERES UV900C |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
Applicant | BIO-TEK INSTRUMENTS, INC. HIGHLAND PARK P.O. BOX 998 Winooski, VT 05404 -0998 |
Contact | Michael N Sevingy |
Correspondent | Michael N Sevingy BIO-TEK INSTRUMENTS, INC. HIGHLAND PARK P.O. BOX 998 Winooski, VT 05404 -0998 |
Product Code | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-06-21 |
Decision Date | 1995-02-06 |