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FDA 510(k)

METAL URETERAL BASKET STONE DISLODGER

K-Number: K934675 · 1994-01-07

Decision Date1994-01-07
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

METAL URETERAL BASKET STONE DISLODGER 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 1994-01-07 under 510(k) number K934675. The device is classified under product code FFL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METAL URETERAL BASKET STONE DISLODGER?

METAL URETERAL BASKET STONE DISLODGER is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Annex Medical, Inc.. The 510(k) number is K934675.

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

METAL URETERAL BASKET STONE DISLODGER received FDA 510(k) clearance on 1994-01-07, under 510(k) number K934675.

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

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?

The FDA product code for METAL URETERAL BASKET STONE DISLODGER is FFL.

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: FFL)

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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