Flexsure Obt

FDA 510(k) K961062 · Smithkline Diagnostics, Inc.

Substantially Equivalent

510(k) numberK961062

Submission

Device name
Flexsure Obt
Applicant
Smithkline Diagnostics, Inc.
Sharon Hill, PA, US
Received
March 18, 1996
Decision date
November 6, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KHE – Reagent, Occult Blood
Device class
Class II (moderate risk)
Regulation
21 CFR 864.6550
Specialty
Hematology

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K821884Gastroccult TMKHE · Traditional 10/08/1982SE
K821674Spinchem Acid Phosphatase ReagentCKB · Traditional 06/22/1982SE
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Questions and answers

When was Flexsure Obt cleared by the FDA?

Flexsure Obt (K961062) received a 510(k) decision of Substantially Equivalent on November 6, 1996, 233 days after the submission was received.

What is the product code of K961062?

The FDA product code is KHE – Reagent, Occult Blood, a Class II (moderate risk) device regulated under 21 CFR 864.6550.