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FDA 510(k)

URETERAL STONE DISLODGER

K-Number: K851922 · 1985-08-02

ApplicantInter-Med Corp.
Decision Date1985-08-02
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URETERAL STONE DISLODGER is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med Corp.. It received FDA 510(k) clearance on 1985-08-02 under 510(k) number K851922. 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 URETERAL STONE DISLODGER?

URETERAL STONE DISLODGER is a medical device that received FDA 510(k) clearance on 1985-08-02. The listed applicant is Inter-Med Corp.. The 510(k) number is K851922.

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

URETERAL STONE DISLODGER received FDA 510(k) clearance on 1985-08-02, under 510(k) number K851922.

Who is the listed applicant for URETERAL STONE DISLODGER?

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

What is the FDA product code for URETERAL STONE DISLODGER?

The FDA product code for URETERAL 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.

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Other records listing Inter-Med 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.

K871291AM CATH ESWL STENTK864669AM CATH ESWL STENTK833058GEN. PURPOSE INSTRUMENT TRAYS &

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

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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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