FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VAKU-8 BLOOD COLLECTION NEEDLES

K Number: K090426 · Decision Jun 12, 2009
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
12
Review Days
113

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Basic Information

Device Name
VAKU-8 BLOOD COLLECTION NEEDLES
K Number
K090426
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Myco Medical Supplies, Inc.
Date Received
February 19, 2009
Decision Date
June 12, 2009
Product Code
FMI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMI Needle, Hypodermic, Single Lumen

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Other Clearances by Myco Medical Supplies, Inc.

K Number Device Name
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
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
Search all 12 clearances from Myco Medical Supplies, Inc. →