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

LANCER MSA BUN DIAG. KIT

K Number: K821562 · Decision Jun 11, 1982
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
116
Applicant Total
191
Review Days
17

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Basic Information

Device Name
LANCER MSA BUN DIAG. KIT
K Number
K821562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1770
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Sherwood Medical Co.
Date Received
May 25, 1982
Decision Date
June 11, 1982
Product Code
CDQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CDQ Urease And Glutamic Dehydrogenase, Urea Nitrogen

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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. →