510(k) K890837

RIA-GNOST INSULIN by Cambridge Medical Technology — Product Code CFP

K890837 is an FDA 510(k) premarket notification submitted by Cambridge Medical Technology for the device "RIA-GNOST INSULIN". The FDA issued a decision of Substantially Equivalent on April 26, 1989. The device falls under product code CFP (Radioimmunoassay, Immunoreactive Insulin), a Class I device regulated under 21 CFR 862.1405. Cambridge Medical Technology has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 1989
Date Received
February 21, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Immunoreactive Insulin
Device Class
Class I
Regulation Number
862.1405
Review Panel
CH
Submission Type