510(k) K823053

NML-TETRA-TUBE RIA by Nuclear Medical Laboratories, Inc. — Product Code CDX

K823053 is an FDA 510(k) premarket notification submitted by Nuclear Medical Laboratories, Inc. for the device "NML-TETRA-TUBE RIA". The FDA issued a decision of Substantially Equivalent on November 10, 1982. The device falls under product code CDX (Radioimmunoassay, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Nuclear Medical Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 10, 1982
Date Received
October 18, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Total Thyroxine
Device Class
Class II
Regulation Number
862.1700
Review Panel
CH
Submission Type