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SURGITEK ENDOTRACHEAL TUBE, LASER RESIS

Page Type
Cleared 510(K)
510(k) Number
K823757
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1983
Days to Decision
135 days

SURGITEK ENDOTRACHEAL TUBE, LASER RESIS

Page Type
Cleared 510(K)
510(k) Number
K823757
510(k) Type
Traditional
Applicant
MEDICAL ENGINEERING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1983
Days to Decision
135 days