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SYNTERMED LIVE

Page Type
Cleared 510(K)
510(k) Number
K070089
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
52 days
Submission Type
Summary

SYNTERMED LIVE

Page Type
Cleared 510(K)
510(k) Number
K070089
510(k) Type
Traditional
Applicant
SYNTERMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
52 days
Submission Type
Summary