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

BUTTERFLY NON-CORING NEEDLE SET

K Number: K863606 · Decision Dec 18, 1986
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
8
Review Days
93

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Basic Information

Device Name
BUTTERFLY NON-CORING NEEDLE SET
K Number
K863606
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Cormed, Inc., Sub. C.R.Bard, Inc.
Date Received
September 16, 1986
Decision Date
December 18, 1986
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

Similar 510(k) Clearances

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Other Clearances by Cormed, Inc., Sub. C.R.Bard, Inc.

K Number Device Name
K860432 PERCUTANEOUS INTRODUCER KIT
K854019 PORT-GARD
K850967 STERILE CORMED MEDIPORT
K850674 CORMED II AMBULATORY INFUSION PUMP
K843083 CORMED HUBER POINT NEEDLE
K833915 VASCULAR ACCESS CATH. REPAIR KIT
K823553 CORCATH H & B VASCULAR ACCESS CATHETER