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MODIFIED MODEL 2001 FIBER OPTICS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883881
510(k) Type
Traditional
Applicant
METATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1988
Days to Decision
90 days

MODIFIED MODEL 2001 FIBER OPTICS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883881
510(k) Type
Traditional
Applicant
METATECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1988
Days to Decision
90 days