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

LANCER L-INA BUFFER, POLYMER, WASH SOLU

K Number: K792014 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
10
Applicant Total
62
Review Days
39

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Basic Information

Device Name
LANCER L-INA BUFFER, POLYMER, WASH SOLU
K Number
K792014
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.4540
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Industries
Date Received
October 5, 1979
Decision Date
November 13, 1979
Product Code
JZW
Advisory Committee
Immunology
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
JZW Nephelometer

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Other Clearances by Sherwood Medical Industries

K Number Device Name
K801070 SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES
K801071 LANCER GLUCOSE RATE REAGENT KIT
K792013 LANCER L-INA HUMAN REFERENCE SERUM
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
Search all 62 clearances from Sherwood Medical Industries →