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

TRI-LEVEL NDI CONTROL

K Number: K810906 · Decision Apr 14, 1981
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
22
Review Days
11

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Basic Information

Device Name
TRI-LEVEL NDI CONTROL
K Number
K810906
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Nuclear Diagnostics, Inc.
Date Received
April 3, 1981
Decision Date
April 14, 1981
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

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K872177 TIPSEP-CORTISOL RIA DIAGNOSTIC KIT
K862312 ENZLIPASE, ENZYMATIC LIPASE KIT
K860472 NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESS
K861735 TIPSEP-TBG ASSAY
K852291 TIPSEP DIGOXIN RIA
K833713 SERUM THYROTROPIN ASSAY KIT, TIPSEP-
K823860 NUCLIPASE (I125) PANCREATIC LIPASE
K811558 TSH-P.E.G.
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