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FDA 510(k)

TAPERED CERVICAL DILATOR

K-Number: K840381 · 1984-04-30

ApplicantIntl. Medical Technologies, Inc.
Decision Date1984-04-30
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAPERED CERVICAL DILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Technologies, Inc.. It received FDA 510(k) clearance on 1984-04-30 under 510(k) number K840381. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAPERED CERVICAL DILATOR?

TAPERED CERVICAL DILATOR is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Intl. Medical Technologies, Inc.. The 510(k) number is K840381.

When did TAPERED CERVICAL DILATOR receive FDA 510(k) clearance?

TAPERED CERVICAL DILATOR received FDA 510(k) clearance on 1984-04-30, under 510(k) number K840381.

Who is the listed applicant for TAPERED CERVICAL DILATOR?

The FDA 510(k) record lists Intl. Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAPERED CERVICAL DILATOR?

The FDA product code for TAPERED CERVICAL DILATOR is HHI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Intl. Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K840383MENSTRUAL ASPIRATION KITK840384DIAGNOSTIC DILATATION & MENSTRUAL KITK840380UTERINE SOUNDK840382VACUUM ASPIRATION CATHETER

Related Devices (Code: HHI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171440Berkeley VC-10 Vacuum Curettage SystemGyrus AcmiK030935BERKELEY V-10 VACUUM CURETTAGE SYSTEMAcmi CorporationK983181CYTOPREPCytoprep Inc. Est.K931205MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTERBaxter Healthcare CorpK904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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