Class I Devices

Class I Devices is a regulatory category of medical devices distinguished by presenting the lowest potential risk to patient safety and typically subject to general controls without the need for premarket approval.

1

Publications

21

Citations

5

Authors

6

Institutions

Publications per year

2017–2026

0

Authors

5

  1. CF
    Carola F. van Eck

    University of Pittsburgh, United States

    1 publications · 21 citations

    1

    h-index

  2. FH
    Freddie H. Fu

    University of Pittsburgh, United States

    1 publications · 21 citations

    1

    h-index

  3. JA
    James A. D’Antonio

    Indiana University – Purdue University Indianapolis, United States

    1 publications · 21 citations

    1

    h-index

  4. AF
    Antonia F. Chen

    Brigham and Women's Hospital, United States

    1 publications · 21 citations

    1

    h-index

  5. BA
    Brian A. Klatt

    University of Pittsburgh Medical Center, United States

    1 publications · 21 citations

    1

    h-index

1–5 of 5

Venues

  1. 1

    h-index

1–1