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ISO13485 |
CE Certification |
Ministry of Health G.M.P. Medical Instrument Certificate of Excellence |
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United States F.D.A. 510k(K020783) -
SPECTRUM 9000MB
PDF of 510(k) STATEMENT F.D.A. Device
Listing Database |
People's Republic of China
Registration Certificate for Medical Device
- SPECTRUM 9000MB |
Registration Form of Medical Device
- SPECTRUM 9000MB |
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United States F.D.A. 510k(K102134) - LA1200 |
People's Republic of China
Registration Certificate for Medical Device
- LA1200 |
Registration Form of Medical Device
- LA1200 |
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United States F.D.A. 510k(K082686) - LA400 |
People's Republic of China
Registration Certificate for Medical Device
- LA400 |
Registration Form of Medical Device - LA400 |
