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FDA 510(k)

JANACEK TUBO-UTERINE IMPLANTATION SET

K-Number: K840766 · 1984-04-23

ApplicantCimed Intl., Inc.
Decision Date1984-04-23
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JANACEK TUBO-UTERINE IMPLANTATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Cimed Intl., Inc.. It received FDA 510(k) clearance on 1984-04-23 under 510(k) number K840766. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JANACEK TUBO-UTERINE IMPLANTATION SET?

JANACEK TUBO-UTERINE IMPLANTATION SET is a medical device that received FDA 510(k) clearance on 1984-04-23. The listed applicant is Cimed Intl., Inc.. The 510(k) number is K840766.

When did JANACEK TUBO-UTERINE IMPLANTATION SET receive FDA 510(k) clearance?

JANACEK TUBO-UTERINE IMPLANTATION SET received FDA 510(k) clearance on 1984-04-23, under 510(k) number K840766.

Who is the listed applicant for JANACEK TUBO-UTERINE IMPLANTATION SET?

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

What is the FDA product code for JANACEK TUBO-UTERINE IMPLANTATION SET?

The FDA product code for JANACEK TUBO-UTERINE IMPLANTATION SET is HTD.

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Other records listing Cimed Intl., 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.

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Related Devices (Code: HTD)

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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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