The following data is part of a premarket notification filed by Diamedix Corp. with the FDA for Diamedix Is-toxoplasma Igm Capture Test System.
Device ID | K001707 |
510k Number | K001707 |
Device Name: | DIAMEDIX IS-TOXOPLASMA IGM CAPTURE TEST SYSTEM |
Classification | Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii |
Applicant | DIAMEDIX CORP. 2140 NORTH MIAMI AVE. Miami, FL 33127 |
Contact | Lynne Stirling |
Correspondent | Lynne Stirling DIAMEDIX CORP. 2140 NORTH MIAMI AVE. Miami, FL 33127 |
Product Code | LGD |
CFR Regulation Number | 866.3780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-06-05 |
Decision Date | 2000-07-07 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00817273020143 | K001707 | 000 |
00817273020006 | K001707 | 000 |