MVM 7.5 FRENCH FLEXIBLE HYSTEROSCOPE
K-Number: K990411 · 1999-05-11
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Device Summary
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.
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
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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