Medical Device Manufacturer · US , MD

Clement Clarke, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1979

Total

Cleared

Denied

Clement Clarke, Inc. has 10 FDA 510(k) cleared ophthalmic devices. Based in US.

Historical record: 10 cleared submissions from 1979 to 1996.

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

FDA 510(k) cleared devices by Clement Clarke, Inc.

10 devices

1-10 of 10

Cleared Jul 18, 1996

PERKINS HAND-HELD APPLANATION TONOMETER

Anesthesiology · 289d

VMX MINI-LOG FLOWMETER

K914126 · BZH

Anesthesiology · 539d

PROFESSIONAL INDIRECT OPHTHALMOSCOPE

K912397 · HLI

Ophthalmic · 148d

Cleared Feb 02, 1990

WRIGHT VENTILOMETER VM-1

K895953 · BZG

Anesthesiology · 114d

VISION-STIMULATOR, CAM

K781313 · HPL

Ophthalmic · 179d

Clement Clarke, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Clement Clarke, Inc.

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