Model 1100 Apc(Angioplasty Pressure Controller)

FDA 510(k) K853136 · E.A. Fischione Instrument Mfg.

Substantially Equivalent

510(k) numberK853136

Submission

Device name
Model 1100 Apc(Angioplasty Pressure Controller)
Applicant
E.A. Fischione Instrument Mfg.
Pittsburgh, PA, US
Received
July 26, 1985
Decision date
December 3, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
MAV – Syringe, Balloon Inflation
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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More from Boston Scientific Corp

510(k)DeviceDecision
K841493Model 1000 Apc-Angioplasty PressureDXT · Traditional 06/11/1984SE

Questions and answers

When was Model 1100 Apc(Angioplasty Pressure Controller) cleared by the FDA?

Model 1100 Apc(Angioplasty Pressure Controller) (K853136) received a 510(k) decision of Substantially Equivalent on December 3, 1985, 130 days after the submission was received.

What is the product code of K853136?

The FDA product code is MAV – Syringe, Balloon Inflation, a Class II (moderate risk) device regulated under 21 CFR 870.1650.