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FDA 510(k)

DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER

K-Number: K860946 · 1986-04-03

ApplicantVan-Tec, Inc.
Decision Date1986-04-03
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1986-04-03 under 510(k) number K860946. 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 DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER?

DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 1986-04-03. The listed applicant is Van-Tec, Inc.. The 510(k) number is K860946.

When did DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER receive FDA 510(k) clearance?

DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER received FDA 510(k) clearance on 1986-04-03, under 510(k) number K860946.

Who is the listed applicant for DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER?

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

What is the FDA product code for DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER?

The FDA product code for DAVIS LOOP STONE EXTRACTOR/URETERAL CATHETER is FFL.

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Other records listing Van-Tec, 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.

K880099VAN-TEC BLADDER EVACUATORK880095BERGER PROSTATE CULTURE CYTOLOGY BRUSHK880098VAN-TEC AUTO BIOPSY NEEDLEK880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUPK880094VAN-TEC ENDOPYELOTOMY KNIFEK874112VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER

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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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