Medical Device Manufacturer · US , Walker , MI

Myocure, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1982

Total

Cleared

Denied

Myocure, Inc. has 15 FDA 510(k) cleared ophthalmic devices. Based in Walker, US.

Historical record: 15 cleared submissions from 1982 to 1988.

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) Regulatory Record - Myocure, Inc.

15 devices

1-15 of 15

ANESTHESIA/RETROBULBAR NEEDLES

K880347 · HMX

Ophthalmic · 98d

Cleared Dec 23, 1987

OPHTHALMIC TIP & BLADE SCALPELS

K874057 · HNN

Ophthalmic · 79d

Cleared Dec 22, 1987

OPHTHALMIC DISPOSABLE BLADES

K874056 · HNN

Ophthalmic · 78d

Cleared Sep 21, 1987

OPHTHALMIC PHACO-BLADE

General & Plastic Surgery · 12d

Cleared Oct 20, 1986

OPHTHALMIC SURGICAL DRAPE

K863662

Ophthalmic · 32d

Cleared Oct 20, 1986

OPHTHALMIC SURGICAL OCULAR MARKERS

OPHTHALMIC SURGICAL SPECULUM

MYOPACH ULTRASONIC PACHOMETER

K844112 · IYO

Radiology · 450d

Cleared Nov 04, 1985

OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE

General & Plastic Surgery · 16d

Myocure, Inc. - FDA 510(k) Cleared Devices

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