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VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND

Page Type
Cleared 510(K)
510(k) Number
K090214
510(k) Type
Abbreviated
Applicant
VERATHON INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2009
Days to Decision
43 days
Submission Type
Summary

VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND

Page Type
Cleared 510(K)
510(k) Number
K090214
510(k) Type
Abbreviated
Applicant
VERATHON INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2009
Days to Decision
43 days
Submission Type
Summary