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

ARGYLE DELEE SUCTION CATHETER W/MUCOUS

K Number: K820572 · Decision Apr 9, 1982
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
3
Applicant Total
191
Review Days
38

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Basic Information

Device Name
ARGYLE DELEE SUCTION CATHETER W/MUCOUS
K Number
K820572
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Sherwood Medical Co.
Date Received
March 2, 1982
Decision Date
April 9, 1982
Product Code
KTR
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KTR Tube, Aspirating, Bronchoscope, Rigid

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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. →