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KAISHOU VAGINAL SPECULUM

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