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

ARGYLE TURKEL SAFETY TROCAR THORACIC CATHETER

K Number: K933510 · Decision Feb 24, 1994
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
16
Applicant Total
191
Review Days
219

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Basic Information

Device Name
ARGYLE TURKEL SAFETY TROCAR THORACIC CATHETER
K Number
K933510
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sherwood Medical Co.
Date Received
July 20, 1993
Decision Date
February 24, 1994
Product Code
GBW
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
GBW Catheter, Peritoneal

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Other Clearances by Sherwood Medical Co.

K Number Device Name
K981365 MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONS
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
K954525 SENSI-TOUCH EPIDURAL ANESTHESIA FILTER
K950201 ARGYLE(R) HYDROPHILIC COATED THORACIC CATHETER
Search all 191 clearances from Sherwood Medical Co. →