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TYMPANOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K953802
510(k) Type
Traditional
Applicant
BLUFF CITY MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/1995
Days to Decision
78 days
Submission Type
Summary

TYMPANOSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K953802
510(k) Type
Traditional
Applicant
BLUFF CITY MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/1995
Days to Decision
78 days
Submission Type
Summary