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Myocure, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K880345CYSTOTOMES/KNIFESMay 3, 1988
K880346CANNULASMay 3, 1988
K880347ANESTHESIA/RETROBULBAR NEEDLESMay 3, 1988
K874057OPHTHALMIC TIP & BLADE SCALPELSDecember 23, 1987
K874056OPHTHALMIC DISPOSABLE BLADESDecember 22, 1987
K873385OPHTHALMIC PHACO-BLADESeptember 21, 1987
K864371SURGICAL SKIN MARKERNovember 17, 1986
K863666THE SAVER KITOctober 20, 1986
K863663OPHTHALMIC SURGICAL OCULAR MARKERSOctober 20, 1986
K863662OPHTHALMIC SURGICAL DRAPEOctober 20, 1986
K863664OPHTHALMIC SURGICAL SPECULUMSeptember 25, 1986
K863665THE ULTIMATESeptember 25, 1986
K844112MYOPACH ULTRASONIC PACHOMETERJanuary 16, 1986
K853598OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDENovember 4, 1985
K822392MYOCUR BLADE PACAugust 25, 1982