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FDA 510(k)

GIP/MED-GLOBE STONE EXTRACTOR BASKETS

K-Number: K942005 · 1994-11-22

Decision Date1994-11-22
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GIP/MED-GLOBE STONE EXTRACTOR BASKETS 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 1994-11-22 under 510(k) number K942005. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GIP/MED-GLOBE STONE EXTRACTOR BASKETS?

GIP/MED-GLOBE STONE EXTRACTOR BASKETS is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Medi-Globe Corp.. The 510(k) number is K942005.

When did GIP/MED-GLOBE STONE EXTRACTOR BASKETS receive FDA 510(k) clearance?

GIP/MED-GLOBE STONE EXTRACTOR BASKETS received FDA 510(k) clearance on 1994-11-22, under 510(k) number K942005.

Who is the listed applicant for GIP/MED-GLOBE STONE EXTRACTOR BASKETS?

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 GIP/MED-GLOBE STONE EXTRACTOR BASKETS?

The FDA product code for GIP/MED-GLOBE STONE EXTRACTOR BASKETS is LQR.

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 Medi-Globe 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 18 devices →

Related Devices (Code: LQR)

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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