510(k) K853401

CHLAMYSET ANTIGEN by Orion Corp. — Product Code LJP

K853401 is an FDA 510(k) premarket notification submitted by Orion Corp. for the device "CHLAMYSET ANTIGEN". The FDA issued a decision of Substantially Equivalent on April 28, 1986. The device falls under product code LJP (Antiserum, Fluorescent, Chlamydia Trachomatis), a Class I device regulated under 21 CFR 866.3120. Orion Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 28, 1986
Date Received
August 12, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antiserum, Fluorescent, Chlamydia Trachomatis
Device Class
Class I
Regulation Number
866.3120
Review Panel
MI
Submission Type