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SEGMENTED VAGINAL APPLICATOR

Page Type
Cleared 510(K)
510(k) Number
K993472
510(k) Type
Traditional
Applicant
MICK RADIO-NUCLEAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
90 days
Submission Type
Summary

SEGMENTED VAGINAL APPLICATOR

Page Type
Cleared 510(K)
510(k) Number
K993472
510(k) Type
Traditional
Applicant
MICK RADIO-NUCLEAR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2000
Days to Decision
90 days
Submission Type
Summary