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

SENSI-TOUCH EPIDURAL ANESTHESIA FILTER

K Number: K954525 · Decision Jan 19, 1996
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
191
Review Days
112

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Basic Information

Device Name
SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
K Number
K954525
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sherwood Medical Co.
Date Received
September 29, 1995
Decision Date
January 19, 1996
Product Code
BXN
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BXN Stimulator, Nerve, Battery-Powered

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Other Clearances by Sherwood Medical Co.

K Number Device Name
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K960982 MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULA
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
K950201 ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER
K954300 ARGYLE NEO-SERT HYDROPHILIC POLYURETHANE UMBILICAL VESSEL CATHETER INSERTION TRAY
Search all 191 clearances from Sherwood Medical Co. →