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KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902193
510(k) Type
Traditional
Applicant
KEVTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1991
Days to Decision
303 days

KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902193
510(k) Type
Traditional
Applicant
KEVTEK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1991
Days to Decision
303 days