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FDA 510(k)

MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER

K-Number: K910742 · 1992-01-14

Decision Date1992-01-14
Product CodeKXO
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1992-01-14 under 510(k) number K910742. The device is classified under product code KXO. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER?

MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER is a medical device that received FDA 510(k) clearance on 1992-01-14. The listed applicant is Graphic Controls Corp.. The 510(k) number is K910742.

When did MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER receive FDA 510(k) clearance?

MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER received FDA 510(k) clearance on 1992-01-14, under 510(k) number K910742.

Who is the listed applicant for MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER?

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

What is the FDA product code for MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER?

The FDA product code for MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER is KXO.

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.

Other records listing Graphic Controls 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.

View all 55 devices →

Related Devices (Code: KXO)

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.

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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