Medical Device Manufacturer · SE , 372 21 Ronneby

Althin Medical AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1999

Recent clearances: A-22 HEMODIALYZER, AF-180 HEMODIALYZER, AF-150 HEMODIALYZER

7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Althin Medical AB Gastroenterology & Urology ✕

7 devices
1-7 of 7
Cleared Jan 18, 2000
A-22 HEMODIALYZER
K992563 · KDI
Gastroenterology & Urology · 169d
Cleared Jan 18, 2000
AF-180 HEMODIALYZER
K992564 · KDI
Gastroenterology & Urology · 169d
Cleared Jan 18, 2000
AF-150 HEMODIALYZER
K992566 · KDI
Gastroenterology & Urology · 169d
Cleared Jan 18, 2000
AF-220 HEMODIALYZER
K992573 · KDI
Gastroenterology & Urology · 169d
Cleared Sep 24, 1999
A-15 HEMODIALYZER
K992594 · FJI
Gastroenterology & Urology · 52d
Cleared Sep 23, 1999
A-18 HEMODIALYZER
K992565 · FJI
Gastroenterology & Urology · 52d
Cleared Apr 15, 1999
ALTHIN MEDICAL AB ALTRACART II
K990010 · KPO
Gastroenterology & Urology · 101d
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