510(k) K101388

FASTPACK TESTO IMMUNOASSAY by Qualigen, Inc. — Product Code CDZ

K101388 is an FDA 510(k) premarket notification submitted by Qualigen, Inc. for the device "FASTPACK TESTO IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on February 18, 2011. The device falls under product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone), a Class I device regulated under 21 CFR 862.1680. Qualigen, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 2011
Date Received
May 17, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Testosterones And Dihydrotestosterone
Device Class
Class I
Regulation Number
862.1680
Review Panel
CH
Submission Type