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FDA 510(k)

VACUUM ASPIRATION CATHETER

K-Number: K840382 · 1984-04-30

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

Device Summary

VACUUM ASPIRATION CATHETER 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 K840382. 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 VACUUM ASPIRATION CATHETER?

VACUUM ASPIRATION CATHETER 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 K840382.

When did VACUUM ASPIRATION CATHETER receive FDA 510(k) clearance?

VACUUM ASPIRATION CATHETER received FDA 510(k) clearance on 1984-04-30, under 510(k) number K840382.

Who is the listed applicant for VACUUM ASPIRATION CATHETER?

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 VACUUM ASPIRATION CATHETER?

The FDA product code for VACUUM ASPIRATION CATHETER 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 KITK840381TAPERED CERVICAL DILATORK840384DIAGNOSTIC DILATATION & MENSTRUAL KITK840380UTERINE SOUND

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

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

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