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FLEX NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K961049
510(k) Type
Traditional
Applicant
LIGHTHOUSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/1996
Days to Decision
187 days
Submission Type
Summary

FLEX NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K961049
510(k) Type
Traditional
Applicant
LIGHTHOUSE MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/1996
Days to Decision
187 days
Submission Type
Summary