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NDYAG LASER TRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K880960
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1988
Days to Decision
52 days

NDYAG LASER TRACHEAL TUBE

Page Type
Cleared 510(K)
510(k) Number
K880960
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1988
Days to Decision
52 days