510(k) K844181

ACTH RIA by Syncor Intl. Corp. — Product Code CKG

K844181 is an FDA 510(k) premarket notification submitted by Syncor Intl. Corp. for the device "ACTH RIA". The FDA issued a decision of Substantially Equivalent on November 27, 1984. The device falls under product code CKG (Radioimmunoassay, Acth), a Class II device regulated under 21 CFR 862.1025. Syncor Intl. Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 27, 1984
Date Received
October 26, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Acth
Device Class
Class II
Regulation Number
862.1025
Review Panel
CH
Submission Type