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FDA 510(k)

METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE

K-Number: K914112 · 1992-02-28

Decision Date1992-02-28
Product CodeFGO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Annex Medical, Inc.. It received FDA 510(k) clearance on 1992-02-28 under 510(k) number K914112. The device is classified under product code FGO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE?

METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE is a medical device that received FDA 510(k) clearance on 1992-02-28. The listed applicant is Annex Medical, Inc.. The 510(k) number is K914112.

When did METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE receive FDA 510(k) clearance?

METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE received FDA 510(k) clearance on 1992-02-28, under 510(k) number K914112.

Who is the listed applicant for METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE?

The FDA 510(k) record lists Annex Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE?

The FDA product code for METAL URETERAL BASKET STONE DISLODGER, FLAT WIRE is FGO.

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 Annex Medical, Inc. 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 23 devices →

Related Devices (Code: FGO)

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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