510(k) K953605

ULTRA-SENSITIVE ESTRADIOL by Diagnostic Systems Laboratories, Inc. — Product Code CHP

K953605 is an FDA 510(k) premarket notification submitted by Diagnostic Systems Laboratories, Inc. for the device "ULTRA-SENSITIVE ESTRADIOL". The FDA issued a decision of Substantially Equivalent on October 2, 1995. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Diagnostic Systems Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1995
Date Received
August 2, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Estradiol
Device Class
Class I
Regulation Number
862.1260
Review Panel
CH
Submission Type