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SINGLE CHANNEL NONFADE OSCILLOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K822517
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
25 days

SINGLE CHANNEL NONFADE OSCILLOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K822517
510(k) Type
Traditional
Applicant
QUINTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
25 days