Disposable Coronary Control Syringe 12CC

FDA 510(k) K875196 · Merit Medical Systems, Inc.

Substantially Equivalent

510(k) numberK875196

Submission

Device name
Disposable Coronary Control Syringe 12CC
Applicant
Merit Medical Systems, Inc.
Salt Lake City, UT, US
Received
December 17, 1987
Decision date
February 11, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXT – Injector And Syringe, Angiographic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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Questions and answers

When was Disposable Coronary Control Syringe 12CC cleared by the FDA?

Disposable Coronary Control Syringe 12CC (K875196) received a 510(k) decision of Substantially Equivalent on February 11, 1988, 56 days after the submission was received.

What is the product code of K875196?

The FDA product code is DXT – Injector And Syringe, Angiographic, a Class II (moderate risk) device regulated under 21 CFR 870.1650.