FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MONOJECT SAMPLETTE SEPARATOR TUBE

K Number: K941291 · Decision Oct 27, 1994
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
21
Applicant Total
191
Review Days
224

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Basic Information

Device Name
MONOJECT SAMPLETTE SEPARATOR TUBE
K Number
K941291
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.6150
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sherwood Medical Co.
Date Received
March 17, 1994
Decision Date
October 27, 1994
Product Code
GIO
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
GIO Tube, Collection, Capillary Blood

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Other Clearances by Sherwood Medical Co.

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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. →