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FDA 510(k)

MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE

K-Number: K990411 · 1999-05-11

Decision Date1999-05-11
Product CodeHIH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 1999-05-11 under 510(k) number K990411. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE?

MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE is a medical device that received FDA 510(k) clearance on 1999-05-11. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K990411.

When did MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE receive FDA 510(k) clearance?

MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE received FDA 510(k) clearance on 1999-05-11, under 510(k) number K990411.

Who is the listed applicant for MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE?

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

What is the FDA product code for MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE?

The FDA product code for MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE is HIH.

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 Karl Storz Endoscopy 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 35 devices →

Related Devices (Code: HIH)

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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