510(k) K831292

ANTI-ENA TEST by Meloy Laboratories, Inc. — Product Code LKO

K831292 is an FDA 510(k) premarket notification submitted by Meloy Laboratories, Inc. for the device "ANTI-ENA TEST". The FDA issued a decision of Substantially Equivalent on July 18, 1983. The device falls under product code LKO (Anti-Rnp Antibody, Antigen And Control), a Class II device regulated under 21 CFR 866.5100. Meloy Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 1983
Date Received
April 20, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Anti-Rnp Antibody, Antigen And Control
Device Class
Class II
Regulation Number
866.5100
Review Panel
IM
Submission Type