The following data is part of a premarket notification filed by Pro-lab, Inc. with the FDA for D'ala Rapid Test.
Device ID | K861889 |
510k Number | K861889 |
Device Name: | D'ALA RAPID TEST |
Classification | Discs, Strips And Reagents, Microorganism Differentiation |
Applicant | PRO-LAB, INC. 76 GLENGARRY AVENUE TORONTO Ontario Canada M5m 1c9, CA |
Contact | Lynn Rae |
Correspondent | Lynn Rae PRO-LAB, INC. 76 GLENGARRY AVENUE TORONTO Ontario Canada M5m 1c9, CA |
Product Code | JTO |
CFR Regulation Number | 866.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-05-16 |
Decision Date | 1986-06-03 |