Last synced on 14 November 2025 at 11:06 pm

KENSTONE

Page Type
Cleared 510(K)
510(k) Number
K990139
510(k) Type
Traditional
Applicant
KENDA USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1999
Days to Decision
100 days
Submission Type
Summary

KENSTONE

Page Type
Cleared 510(K)
510(k) Number
K990139
510(k) Type
Traditional
Applicant
KENDA USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1999
Days to Decision
100 days
Submission Type
Summary