The following data is part of a premarket notification filed by Artel, Inc. with the FDA for Mp Mini Photometer.
Device ID | K914809 |
510k Number | K914809 |
Device Name: | MP MINI PHOTOMETER |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | ARTEL, INC. 12 DEPOT ST. Windham, ME 04062 |
Contact | Charles Ewing |
Correspondent | Charles Ewing ARTEL, INC. 12 DEPOT ST. Windham, ME 04062 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-25 |
Decision Date | 1992-01-27 |