Myocure, Inc.
Myocure, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1988.
Top product codes for Myocure, Inc.
Recent clearances by Myocure, Inc.
- K880345 — CYSTOTOMES/KNIFES
- K880346 — CANNULAS
- K880347 — ANESTHESIA/RETROBULBAR NEEDLES
- K874057 — OPHTHALMIC TIP & BLADE SCALPELS
- K874056 — OPHTHALMIC DISPOSABLE BLADES
- K873385 — OPHTHALMIC PHACO-BLADE
- K864371 — SURGICAL SKIN MARKER
- K863662 — OPHTHALMIC SURGICAL DRAPE
- K863663 — OPHTHALMIC SURGICAL OCULAR MARKERS
- K863666 — THE SAVER KIT
- K863664 — OPHTHALMIC SURGICAL SPECULUM
- K863665 — THE ULTIMATE
- K844112 — MYOPACH ULTRASONIC PACHOMETER
- K853598 — OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE
- K822392 — MYOCUR BLADE PAC
Data sourced from openFDA. This site is unofficial and independent of the FDA.