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

LANCER L-INA HUMAN REFERENCE SERUM

K Number: K792013 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
107
Registration Numbers
107
Same Product Code
301
Applicant Total
62
Review Days
39

Basic Information

Device Name
LANCER L-INA HUMAN REFERENCE SERUM
K Number
K792013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
SHERWOOD MEDICAL INDUSTRIES
Date Received
October 5, 1979
Decision Date
November 13, 1979
Product Code
JIX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JIX Calibrator, Multi-Analyte Mixture

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K782077 LANCER ICE CUBE
K790523 ARGYLE ESOPHAGEAL STETHOSCOPE
K790196 MONOJECT ARTERIAL BLOOD SAMPLING DEVICE
K790197 REAGENT KIT, LANCER GLUCOSE
K781459 MONOJECT SCALE MAGNIFIER
K781060 MONOJECT ENDOSSEOUS DENTAL IMPLANT
K772149 LANCER BIOPSY HOLDER
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