Medical Device Manufacturer · US , Mchenry , IL

Vanaray Laboratories, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1980

Total

Cleared

Denied

Vanaray Laboratories, Inc. has 10 FDA 510(k) cleared neurology devices. Based in Mchenry, US.

Historical record: 10 cleared submissions from 1980 to 1981.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vanaray Laboratories, Inc.

10 devices

1-10 of 10

Cleared Jan 08, 1981

ECA GEL PROUDUCT REFORMULATION

K802647 · GYB

Neurology · 80d

Cleared Nov 26, 1980

UCA CREAM PRODUCT REFORMULATION

K802648 · GYB

Neurology · 37d

Cleared Nov 12, 1980

UCA GEL PRODUCT REFORMAULATION

K802649 · GYB

Neurology · 23d

Cleared Nov 12, 1980

UCA LOTION PRODUCT REFORMULATION

K802650 · GYB

Neurology · 23d

Cleared Jun 17, 1980

ECA CREAM REFORMULATION

Vanaray Laboratories, Inc. - FDA 510(k) Cleared Devices

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