Grieshaber & Co.
Grieshaber & Co. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1995.
Top product codes for Grieshaber & Co.
Recent clearances by Grieshaber & Co.
- K950056 — THE GRIESHABER AXIAL CUTTER
- K930842 — THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE
- K914588 — GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE
- K914587 — GRIESHABER AIR/FLUID TUBING SET
- K914585 — GRIESHABER TWO FUNCTION MANIPULATOR
- K914586 — GRIESHABER THREE FUNCTION MANIPULATOR
- K897119 — GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
- K900714 — ZZIPP INSTANT BOVIE CLEANER
- K890782 — GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)
- K890783 — GRIESHABER VISCOELASTIC INJECTION SYSTEM
- K884043 — GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE
- K863444 — GRIESHABER GLOBAL CONTROL TUBING SET
- K864056 — GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT
- K860479 — GREEN-LINE BIPOLAR COAGULATION UNIT
- K860502 — G.A.S./GRIESHABER AIR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.