21 C.F.R. · Food and Drugs
21 C.F.R. § 870.1255

Balloon aortic valvuloplasty catheter.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 870.1255 — Balloon aortic valvuloplasty catheter.

§ 870.1255 Balloon aortic valvuloplasty catheter. (a) Identification. A balloon aortic valvuloplasty catheter is a catheter with a balloon at the distal end of the shaft, which is intended to treat stenosis in the aortic valve when the balloon is expanded. (b) Classification. Class II (special controls). The special controls for this device are: (1) The device must be demonstrated to be biocompatible. (2) Sterility and shelf life testing must demonstrate the sterility of patient-contacting components and the shelf life of these components. (3) Non-clinical performance evaluation must demonstrate that the device performs as intended under anticipated conditions of use, including device delivery, inflation, deflation, and removal. (4) In vivo evaluation of the device must demonstrate device performance, including the ability of the device to treat aortic stenosis. (5) Labeling must include a detailed summary of the device-related and procedure-related complications pertinent to the use of the device. [82 FR 34852, July 27, 2017]

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 870.1255
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The regulatory text of 21 C.F.R. § 870.1255 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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