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FDA 510(k)

UTERINE MANIPULATOR 4.5MM

K-Number: K841681 · 1984-04-23

ApplicantHumi Corp.
Decision Date1984-04-23
Product Code
DecisionUnknown

Device Summary

UTERINE MANIPULATOR 4.5MM is the device name listed in this FDA 510(k) record. The listed applicant is Humi Corp.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K841681. FDA Decision: Unknown.

Frequently Asked Questions

What is the UTERINE MANIPULATOR 4.5MM?

UTERINE MANIPULATOR 4.5MM is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Humi Corp.. The 510(k) number is K841681.

When did UTERINE MANIPULATOR 4.5MM receive FDA 510(k) clearance?

UTERINE MANIPULATOR 4.5MM received FDA 510(k) clearance on 1984-04-23, under 510(k) number K841681.

Who is the listed applicant for UTERINE MANIPULATOR 4.5MM?

The FDA 510(k) record lists Humi Corp. as the applicant. This does not by itself establish the device manufacturer.

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 Humi Corp. 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.

K841682UTERINE INJECTOR 4.0MM

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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