The following data is part of a premarket notification filed by Diagnostic Chemicals, Ltd. (usa) with the FDA for Dc-uibc-cal.
Device ID | K925877 |
510k Number | K925877 |
Device Name: | DC-UIBC-CAL |
Classification | Calibrator, Primary |
Applicant | DIAGNOSTIC CHEMICALS, LTD. (USA) 16 FIRST ST. WEST ROYALTY INDUSTRIAL PARK Charlottestown,pei,canada, CA C1e 1b0 |
Contact | Karen Callbeck |
Correspondent | Karen Callbeck DIAGNOSTIC CHEMICALS, LTD. (USA) 16 FIRST ST. WEST ROYALTY INDUSTRIAL PARK Charlottestown,pei,canada, CA C1e 1b0 |
Product Code | JIS |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-11-19 |
Decision Date | 1993-03-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00628063400478 | K925877 | 000 |