Usci (R) Disposable Inflation Device

FDA 510(k) K863037 · C.R. Bard, Inc.

Substantially Equivalent

510(k) numberK863037

Submission

Device name
Usci (R) Disposable Inflation Device
Applicant
C.R. Bard, Inc.
Murray Hill, NJ, US
Received
August 12, 1986
Decision date
September 23, 1986
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 Usci (R) Disposable Inflation Device cleared by the FDA?

Usci (R) Disposable Inflation Device (K863037) received a 510(k) decision of Substantially Equivalent on September 23, 1986, 42 days after the submission was received.

What is the product code of K863037?

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