Medical Instrument Development Laboratories, Inc.
Medical Instrument Development Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 2011.
Top product codes for Medical Instrument Development Laboratories, Inc.
Recent clearances by Medical Instrument Development Laboratories, Inc.
- K102222 — ULTIMATE VIT ENHAMCER (UVE)
- K020911 — MID LABS AUTONOMOUS VIT ENHANCER (AVE)
- K992943 — VIT ENHANCER
- K971067 — DIGI-INJECTOR
- K950287 — UNIVIT PROBE
- K934600 — MICRODRIVE
- K932669 — SUPRA-VIT(TM)
- K932131 — MID LABS TWIN ILLUMINATOR
- K924222 — MID LABS, INC. VIT MATE
- K851610 — COMBINED MVS SYSTEMS
- K851009 — INFUSION SLEEVE - OPHTHALMIC
- K850857 — I/A HANDPIECE
- K844761 — SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD
- K842793 — MVS XII
- K843391 — INFUSION ASPIRATION VITRECTOMY SYS
- K844131 — NUCLEOTOME
- K842471 — AUTOMATED INTRAOCULAR SCISSORS
- K834537 — MICRO VIT FRAGMENTATION SYSTEM
- K831584 — BAILEY ASPIRATOR/IRRIGATOR
- K831192 — INFUSION CANNULA
- K831193 — SCLERAL PLUG
- K820026 — VITRE CON
Data sourced from openFDA. This site is unofficial and independent of the FDA.