Medical Device Manufacturer · US , Oceanside , CA

Viramed Biotech AG - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2005

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.

FDA 510(k) cleared devices by Viramed Biotech AG

7 devices

1-7 of 7

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