510(k) K820741

MR1 LUTROPIN RIA KIT by Microanalytic Research, Inc. — Product Code CEP

K820741 is an FDA 510(k) premarket notification submitted by Microanalytic Research, Inc. for the device "MR1 LUTROPIN RIA KIT". The FDA issued a decision of Substantially Equivalent on April 14, 1982. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Microanalytic Research, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 14, 1982
Date Received
March 18, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Luteinizing Hormone
Device Class
Class I
Regulation Number
862.1485
Review Panel
CH
Submission Type