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ENDOTRACHEAL TUBE HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942395
510(k) Type
Traditional
Applicant
S.T.I. MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1994
Days to Decision
42 days
Submission Type
Statement

ENDOTRACHEAL TUBE HOLDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942395
510(k) Type
Traditional
Applicant
S.T.I. MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1994
Days to Decision
42 days
Submission Type
Statement