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NEUSTEIN LARYNGOSCOPE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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