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KAISHOU VAGINAL SPECULUM

Page Type
Cleared 510(K)
510(k) Number
K030761
510(k) Type
Traditional
Applicant
JIANGSU KAISHOU MEDICAL APPARATUS CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/9/2003
Days to Decision
90 days
Submission Type
Statement

KAISHOU VAGINAL SPECULUM

Page Type
Cleared 510(K)
510(k) Number
K030761
510(k) Type
Traditional
Applicant
JIANGSU KAISHOU MEDICAL APPARATUS CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/9/2003
Days to Decision
90 days
Submission Type
Statement