The following data is part of a premarket notification filed by Diagnostic Chemicals, Ltd. (usa) with the FDA for Acid Phosphatase (kinetic) Cat. # 320-06.
Device ID | K875209 |
510k Number | K875209 |
Device Name: | ACID PHOSPHATASE (KINETIC) CAT. # 320-06 |
Classification | Acid Phosphatase, Naphthyl Phosphate |
Applicant | DIAGNOSTIC CHEMICALS, LTD. (USA) 435 MAIN ST. Monroe, CT 06468 |
Contact | Karen Callbeck |
Correspondent | Karen Callbeck DIAGNOSTIC CHEMICALS, LTD. (USA) 435 MAIN ST. Monroe, CT 06468 |
Product Code | CKB |
CFR Regulation Number | 862.1020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-12-18 |
Decision Date | 1988-02-01 |