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FDA 510(k)

ANGIOMED URETERAL STONE DISLODGERS

K-Number: K854652 · 1986-02-10

ApplicantAngiomed U.S., Inc.
Decision Date1986-02-10
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ANGIOMED URETERAL STONE DISLODGERS is the device name listed in this FDA 510(k) record. The listed applicant is Angiomed U.S., Inc.. It received FDA 510(k) clearance on 1986-02-10 under 510(k) number K854652. 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 ANGIOMED URETERAL STONE DISLODGERS?

ANGIOMED URETERAL STONE DISLODGERS is a medical device that received FDA 510(k) clearance on 1986-02-10. The listed applicant is Angiomed U.S., Inc.. The 510(k) number is K854652.

When did ANGIOMED URETERAL STONE DISLODGERS receive FDA 510(k) clearance?

ANGIOMED URETERAL STONE DISLODGERS received FDA 510(k) clearance on 1986-02-10, under 510(k) number K854652.

Who is the listed applicant for ANGIOMED URETERAL STONE DISLODGERS?

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

What is the FDA product code for ANGIOMED URETERAL STONE DISLODGERS?

The FDA product code for ANGIOMED URETERAL STONE DISLODGERS is FFL.

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Other records listing Angiomed U.S., 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.

K874771ANGIOMED INTRODUCING SETSK874585ANGIOMED OSTY-CUT BONE BIOPSY NEEDLEK864225ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENTK863386VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETSK862805ANGIOMED VAC-U-CUT BIOPSY NEEDLEK863446ANGIOMED HIGH PRESSURE CONNECTORS

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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.

K190492Peralta Stone Removal CatheterCalcula Technologies, Inc.K172299Accordion Piccolo Stone Management DeviceThs International, Inc. D/B/A Accordion MedicalK102887ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510Percutaneous Systems, Inc.K082803COAXIAL ACCORDION STONE MANAGEMENT DEVICE, MODEL: COAC12005 - COA20015Percutaneous Systems, Inc.K052048ACCORDIONPercutaneous Systems, IncorporatedK012581REPROCESSED STONE RETRIEVAL BASKETSSterilmed, Inc.

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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