Wako(Tm) Uibc

FDA 510(k) K875176 · Wako Chemicals USA, Inc.

Substantially Equivalent

510(k) numberK875176

Submission

Device name
Wako(Tm) Uibc
Applicant
Wako Chemicals USA, Inc.
Dallas, TX, US
Received
December 17, 1987
Decision date
February 2, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JQF – Bathophenanthroline, Iron Binding Capacity
Device class
Class I (low risk)
Regulation
21 CFR 862.1415
Specialty
Clinical Chemistry

Other 510(k)s with product code JQF

510(k)DeviceApplicantDecision
K051111Sentinel Uibc LiquidJQF · Traditional Sentinel Ch. Srl11/17/2005SE
K984122Wako L-Type Uibc, Wako Uibc CalibratorJQF · Traditional Wako Chemicals USA, Inc.01/20/1999SE
K863066TransfermeterJQF · Traditional J. D. Assoc.12/04/1986SE
K830032Total Iron Binding Capacity TestJQF · Traditional Sclavo, Inc.01/28/1983SE
K811942J & S Iron Saturating ReagentJQF · Traditional Thyroid Diagnostics, Inc.09/08/1981SE
K810086Iron & TicbJQF · Traditional Bio-Analytics Laboratories, Inc.01/28/1981SE
K792409Elvi Total Iron Binding CapacityJQF · Traditional Volu Sol Medical Industries12/06/1979SE

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Questions and answers

When was Wako(Tm) Uibc cleared by the FDA?

Wako(Tm) Uibc (K875176) received a 510(k) decision of Substantially Equivalent on February 2, 1988, 47 days after the submission was received.

What is the product code of K875176?

The FDA product code is JQF – Bathophenanthroline, Iron Binding Capacity, a Class I (low risk) device regulated under 21 CFR 862.1415.