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KEISEI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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