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FDA 510(k)

MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM

K-Number: K990220 · 1999-03-31

ApplicantMedi-Globe Corp.
Decision Date1999-03-31
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Globe Corp.. It received FDA 510(k) clearance on 1999-03-31 under 510(k) number K990220. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM?

MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-03-31. The listed applicant is Medi-Globe Corp.. The 510(k) number is K990220.

When did MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM receive FDA 510(k) clearance?

MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM received FDA 510(k) clearance on 1999-03-31, under 510(k) number K990220.

Who is the listed applicant for MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM?

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

What is the FDA product code for MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM?

The FDA product code for MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM is FCG.

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Other records listing Medi-Globe Corp. as applicant

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Related Devices (Code: FCG)

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

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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