Dermatological Device Regulation Within The Food And Drug Administration's 510(k) Pathway

Title

Dermatological Device Regulation Within The Food And Drug Administration's 510(k) Pathway

Creator

Ezaldein H; Scott J; Kunzler E; Suggs A; Reichert B A; Leffell D

Publisher

Lasers in Surgery and Medicine

Date

2018
2018-04

Subject

Dermatology; Surgery

Identifier

n/a

Format

Journal Article or Conference Abstract Publication

URL Address

n/a

Search for Full-text

Users with a NEOMED Library login can search for full-text journal articles at the following url: https://libraryguides.neomed.edu/home

Rights

Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).

Pages

380-380

Issue

4

Volume

50

Citation

Ezaldein H; Scott J; Kunzler E; Suggs A; Reichert B A; Leffell D, “Dermatological Device Regulation Within The Food And Drug Administration's 510(k) Pathway,” NEOMED Bibliography Database, accessed April 16, 2021, https://neomed.omeka.net/items/show/9462.

Social Bookmarking