Medical Device Manufacturer · US , Centralia , WA

Vista Labs - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Vista Labs has 2 FDA 510(k) cleared medical devices. Based in Centralia, US.

Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Vista Labs Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vista Labs

2 devices
1-2 of 2
Cleared Aug 05, 1997
V-12 LONG LIFE 675 HEARING AID
K972755 · ESD
Ear, Nose, Throat · 14d
Cleared Jun 06, 1997
VISTA V-38 CIC
K970939 · ESD
Ear, Nose, Throat · 85d
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