510(k) K994424

DIAMEDIX IS-ANTI-DSDNA TEST SYSTEM by Diamedix Corp. — Product Code LRM

K994424 is an FDA 510(k) premarket notification submitted by Diamedix Corp. for the device "DIAMEDIX IS-ANTI-DSDNA TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on February 18, 2000. The device falls under product code LRM (Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control), a Class II device regulated under 21 CFR 866.5100. Diamedix Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 2000
Date Received
December 30, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control
Device Class
Class II
Regulation Number
866.5100
Review Panel
IM
Submission Type