Vision(R) Prothrombin Time

FDA 510(k) K883441 · Abbott Laboratories

Substantially Equivalent

510(k) numberK883441

Submission

Device name
Vision(R) Prothrombin Time
Applicant
Abbott Laboratories
Abbott Park, IL, US
Received
August 15, 1988
Decision date
September 13, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GJS – Test, Time, Prothrombin
Device class
Class II (moderate risk)
Regulation
21 CFR 864.7750
Specialty
Hematology

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Questions and answers

When was Vision(R) Prothrombin Time cleared by the FDA?

Vision(R) Prothrombin Time (K883441) received a 510(k) decision of Substantially Equivalent on September 13, 1988, 29 days after the submission was received.

What is the product code of K883441?

The FDA product code is GJS – Test, Time, Prothrombin, a Class II (moderate risk) device regulated under 21 CFR 864.7750.