Myco Medical Supplies, Inc.
Myco Medical Supplies, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2021, with 2 FDA device recalls on record.
Top product codes for Myco Medical Supplies, Inc.
FDA recalls by Myco Medical Supplies, Inc.
- Z-0444-2016 — Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
- Z-0891-2013 — Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Myco Medical Supplies, Inc.
- K203668 — RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal Needles
- K173279 — RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube Holder
- K090426 — VAKU-8 BLOOD COLLECTION NEEDLES
- K042504 — CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETER
- K000592 — UNOLOK PLUS INFUSION SET AND VAKU-8 PLUS BLOOD COLLECTION SET
- K990519 — PHOENIX EPIDURAL & SPINAL NEEDLES
- K982646 — AILEE SUTURES AND AILEE NEEDLES
- K990388 — TUTOPLUS IV ADMINISTRATION SET
- K982098 — TUTODROP 1 AND TUTODROP 2
- K963364 — GLASS VAN GLASS SYRINGES
- K953252 — DISPOSABLE SCALP VEIN INFUSION SET
- K945225 — DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.