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

LANCER SPECIMEN CONTAINER

K Number: K792156 · Decision Dec 10, 1979
Classifications
1
FEI Numbers
294
Registration Numbers
294
Same Product Code
22
Applicant Total
191
Review Days
42

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Basic Information

Device Name
LANCER SPECIMEN CONTAINER
K Number
K792156
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3250
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Co.
Date Received
October 29, 1979
Decision Date
December 10, 1979
Product Code
FMH
Advisory Committee
Pathology
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FMH Container, Specimen, Sterile

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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. →