TAPERED CERVICAL DILATOR

System, Abortion, Vacuum

INTL. MEDICAL TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Intl. Medical Technologies, Inc. with the FDA for Tapered Cervical Dilator.

Pre-market Notification Details

Device IDK840381
510k NumberK840381
Device Name:TAPERED CERVICAL DILATOR
ClassificationSystem, Abortion, Vacuum
Applicant INTL. MEDICAL TECHNOLOGIES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHHI  
CFR Regulation Number884.5070 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-01-30
Decision Date1984-04-30

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