This page includes the latest FDA filings for Skylark Device Systems Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 8020618 |
| FEI Number | 3008069124 |
| Name | SKYLARK GROUPWIDE INC. |
| Owner & Operator | SKYLARK DEVICE & SYSTEMS CO., LTD |
| Contact Address | 10F, No.201, FU-SING N RD TAIPEI TW-TPE Taipei - Special Municipality 105 TW |
| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2F, NO. 30., WENXING RD TAOYUAN Taipei - Special Municipality, 333 TW |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
SKYLARK DEVICE & SYSTEMS CO., LTD | SKYLARK URO PROBE | 2005-12-05 |
SKYLARK DEVICE & SYSTEMS CO., LTD | BIO-STIM KIT | 2005-09-07 |
SKYLARK DEVICE & SYSTEMS CO., LTD | SD-730 IF-SDS, PERFECT PULSE IF-SDS | 2000-02-03 |