510(k) K040575

PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112 by Phamatech, Inc. — Product Code CGJ

K040575 is an FDA 510(k) premarket notification submitted by Phamatech, Inc. for the device "PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112". The FDA issued a decision of Substantially Equivalent on May 20, 2004. The device falls under product code CGJ (Radioimmunoassay, Follicle-Stimulating Hormone), a Class I device regulated under 21 CFR 862.1300. Phamatech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 20, 2004
Date Received
March 4, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Follicle-Stimulating Hormone
Device Class
Class I
Regulation Number
862.1300
Review Panel
CH
Submission Type