Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K062120Substantially Equivalent

Cisbio Renin Ria Test

Cis Bio International, East Stroudsburg PA / Traditional, Substantially Equivalent

K062120 is the FDA 510(k) clearance record for CISBIO RENIN RIA TEST, a class II device, cleared for Cis Bio International on under FDA product code CIB (Radioimmunoassay, Angiotensin I And Renin). FDA records list one 510(k) clearance for Cis Bio International. As of , FDA records show no recalls naming K062120.

Clearance record

Decision date
Received
(248 days to decision)
Product code
CIB Radioimmunoassay, Angiotensin I And Renin
Regulation
21 CFR 862.1085
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Cis Bio International 150 Cherry Ln. Rd., East Stroudsburg PA
510(k) summary
Statement
Third party review
No

Clearances, product code CIB

Trailing 12 months

FDA records hold no clearances under product code CIB in the trailing twelve months.

FDA records show no clearances under product code CIB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CIB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260