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

MONOJECT VERTICAL ENTRY CHEMOTHERAPY SHARPS CONTAINER

K Number: K951515 · Decision May 23, 1995
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
191
Review Days
50

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Basic Information

Device Name
MONOJECT VERTICAL ENTRY CHEMOTHERAPY SHARPS CONTAINER
K Number
K951515
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sherwood Medical Co.
Date Received
April 3, 1995
Decision Date
May 23, 1995
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 Sherwood Medical Co.

K Number Device Name
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K962880 SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEM
K960574 ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEM
K960677 KANGAROO JEJUNAL FEEDING SYSTEM
K960632 KANGAROO FEEDING TUBE PLACMENT STYLET
K955831 ARGYLE ASPR-CARE CLOSED SUCTION SYSTEM
K954429 KANGAROO ENTRISTAR SKIN-LEVEL GASTROSTOMY KIT
K954525 SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
K950201 ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER
Search all 191 clearances from Sherwood Medical Co. →