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ROWDEN UTERINE MANIPULATOR INJECTOR AND RUMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932115
510(k) Type
Traditional
Applicant
BLAIRDEN PRECISION INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1994
Days to Decision
417 days
Submission Type
Statement

ROWDEN UTERINE MANIPULATOR INJECTOR AND RUMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932115
510(k) Type
Traditional
Applicant
BLAIRDEN PRECISION INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/24/1994
Days to Decision
417 days
Submission Type
Statement