Shenzhen Creative Industry Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shenzhen Creative Industry Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Pulse Oximeter, Patient Monitor, Handheld Pulse Oximeter, Model SP-20
11
Total
11
Cleared
0
Denied
Shenzhen Creative Industry Co., Ltd. has 11 FDA 510(k) cleared medical devices. Based in Flintville, US.
Last cleared in 2021. Active since 2007. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Creative Industry Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Irc and International Regulatory Consultants (Irc).
FDA 510(k) Regulatory Record - Shenzhen Creative Industry Co., Ltd.
11 devices
Cleared
Jan 25, 2021
Pulse Oximeter
Anesthesiology
237d
Cleared
Dec 31, 2019
Patient Monitor
Cardiovascular
125d
Cleared
Nov 13, 2018
Handheld Pulse Oximeter, Model SP-20
Anesthesiology
424d
Cleared
Sep 09, 2017
All-in-One Health Monitor, PC-303
Cardiovascular
247d
Cleared
Jun 03, 2015
Pulse Oximeter, Models PC-66A
Anesthesiology
138d
Cleared
Oct 01, 2013
PATIENT MONITOR
Cardiovascular
301d
Cleared
Dec 07, 2012
PC-60NW FINGERTIP OXIMETER
Anesthesiology
290d
Cleared
Mar 30, 2010
VITAL SIGNS MONITOR
Anesthesiology
182d
Cleared
Feb 06, 2009
MODEL PC-860 FETAL DOPPLER
Obstetrics & Gynecology
200d
Cleared
Jan 10, 2008
PC-180 / PRINCE 180 EASY ECG MONITOR
Cardiovascular
63d
Cleared
Jul 13, 2007
PC-60, NON-INVASIVEPULSE OXIMETER
Anesthesiology
218d