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KEISEI

Page Type
Cleared 510(K)
510(k) Number
K950613
510(k) Type
Traditional
Applicant
KEISEI (USA) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1996
Days to Decision
369 days
Submission Type
Statement

KEISEI

Page Type
Cleared 510(K)
510(k) Number
K950613
510(k) Type
Traditional
Applicant
KEISEI (USA) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1996
Days to Decision
369 days
Submission Type
Statement