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SONOPSY LA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980423
510(k) Type
Traditional
Applicant
NEOVISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1998
Days to Decision
185 days
Submission Type
Summary

SONOPSY LA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K980423
510(k) Type
Traditional
Applicant
NEOVISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1998
Days to Decision
185 days
Submission Type
Summary