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

MONOJECT(R) MONOLETTOR SAFETY LANCET

K Number: K932785 · Decision Sep 29, 1993
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
191
Review Days
112

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Basic Information

Device Name
MONOJECT(R) MONOLETTOR SAFETY LANCET
K Number
K932785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sherwood Medical Co.
Date Received
June 9, 1993
Decision Date
September 29, 1993
Product Code
FMK
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

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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. →