Viramed Biotech AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viramed Biotech AG - FDA 510(k) Cleared Devices
Recent clearances: Viramed Borrela All-In-One ViraChip Test Kit
7
Total
7
Cleared
0
Denied
Viramed Biotech AG has 7 FDA 510(k) cleared medical devices. Based in Oceanside, US.
Last cleared in 2022. Active since 2005. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Viramed Biotech AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Viralab, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Viramed Biotech AG
7 devices
Cleared
Aug 19, 2022
Viramed Borrela All-In-One ViraChip Test Kit
Microbiology
226d
Cleared
Aug 22, 2017
Borrelia B31 ViraChip IgM Test Kit
Microbiology
237d
Cleared
Jul 12, 2017
Borrelia B31 ViraChip IgG Test Kit
Microbiology
210d
Cleared
Nov 25, 2009
VIRAMED BIOTECH AG BORRELIA B31 IGG VIRASTRIPE, MODEL V-BBSGUS
Microbiology
84d
Cleared
Aug 05, 2009
VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE
Microbiology
356d
Cleared
Aug 11, 2005
VIRAMED BIOTECH BORRELIA B31 IGG VIRABLOT
Microbiology
107d
Cleared
Aug 11, 2005
BIRAMED BIOTECH BORRELIA B31 IGM VIRABLOT
Microbiology
104d