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NEUROGAR III

Page Type
Cleared 510(K)
510(k) Number
K812036
510(k) Type
Traditional
Applicant
INTER MED INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
18 days

NEUROGAR III

Page Type
Cleared 510(K)
510(k) Number
K812036
510(k) Type
Traditional
Applicant
INTER MED INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
18 days