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FDA 510(k)

MARION WINDOW

K-Number: K920182 · 1992-03-26

ApplicantTnt Moberg Intl. , Ltd.
Decision Date1992-03-26
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MARION WINDOW is the device name listed in this FDA 510(k) record. The listed applicant is Tnt Moberg Intl. , Ltd.. It received FDA 510(k) clearance on 1992-03-26 under 510(k) number K920182. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARION WINDOW?

MARION WINDOW is a medical device that received FDA 510(k) clearance on 1992-03-26. The listed applicant is Tnt Moberg Intl. , Ltd.. The 510(k) number is K920182.

When did MARION WINDOW receive FDA 510(k) clearance?

MARION WINDOW received FDA 510(k) clearance on 1992-03-26, under 510(k) number K920182.

Who is the listed applicant for MARION WINDOW?

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

What is the FDA product code for MARION WINDOW?

The FDA product code for MARION WINDOW is KGX.

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Related Devices (Code: KGX)

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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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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