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NEUSTEIN LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K901164
510(k) Type
Traditional
Applicant
NEUTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1990
Days to Decision
211 days

NEUSTEIN LARYNGOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K901164
510(k) Type
Traditional
Applicant
NEUTECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/9/1990
Days to Decision
211 days