Medical Device Manufacturer · US , Fallisington , PA

Grieshaber & Co. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1986

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Grieshaber & Co. Ophthalmic ✕

8 devices

1-8 of 8

Cleared May 05, 1995

THE GRIESHABER AXIAL CUTTER

Ophthalmic · 119d

Cleared May 03, 1994

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE

Ophthalmic · 440d

Cleared Jan 23, 1992

GRIESHABER AIR/FLUID TUBING SET

Ophthalmic · 99d

Cleared Apr 12, 1990

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

Ophthalmic · 107d

Cleared Jun 23, 1989

GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)

Ophthalmic · 128d

Cleared Nov 16, 1988

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE

Ophthalmic · 51d

Cleared Oct 31, 1986

GRIESHABER GLOBAL CONTROL TUBING SET

Ophthalmic · 53d

Cleared Oct 31, 1986

GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT

Ophthalmic · 16d