Skylark Device & Systems Co., Ltd. is one of 416 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Skylark Device & Systems Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SKYLARK URO PROBE, BIO-STIM KIT, SKYLARK INFRARED PHOTON STIMULATOR, MODELS, SD-956IR AND SD-100IR
6
Total
6
Cleared
0
Denied
Skylark Device & Systems Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 6 cleared submissions from 2000 to 2005. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Skylark Device & Systems Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Skylark Device & Systems Co., Ltd.
6 devices
Cleared
Dec 05, 2005
SKYLARK URO PROBE
Gastroenterology & Urology
40d
Cleared
Sep 07, 2005
BIO-STIM KIT
Neurology
225d
Cleared
Jun 06, 2005
SKYLARK INFRARED PHOTON STIMULATOR, MODELS, SD-956IR AND SD-100IR
Physical Medicine
187d
Cleared
Nov 18, 2004
SDS-4I
Physical Medicine
330d
Cleared
Aug 06, 2001
CONDUCTIVE GEL FOR ULTRASOUND
Neurology
329d
Cleared
Feb 03, 2000
SD-730 IF-SDS, PERFECT PULSE IF-SDS
Neurology
181d