Anest Iwata Sparmax Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Anest Iwata Sparmax Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Cliq Aspirator
1
Total
1
Cleared
0
Denied
Anest Iwata Sparmax Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Anest Iwata Sparmax Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance Systems International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Anest Iwata Sparmax Co., Ltd.
1 devices