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FDA 510(k)

VAN-TEC POSITIVE OPEN SEGURA BASKET

K-Number: K870615 · 1987-03-25

ApplicantVan-Tec, Inc.
Decision Date1987-03-25
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VAN-TEC POSITIVE OPEN SEGURA BASKET 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 1987-03-25 under 510(k) number K870615. 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 VAN-TEC POSITIVE OPEN SEGURA BASKET?

VAN-TEC POSITIVE OPEN SEGURA BASKET is a medical device that received FDA 510(k) clearance on 1987-03-25. The listed applicant is Van-Tec, Inc.. The 510(k) number is K870615.

When did VAN-TEC POSITIVE OPEN SEGURA BASKET receive FDA 510(k) clearance?

VAN-TEC POSITIVE OPEN SEGURA BASKET received FDA 510(k) clearance on 1987-03-25, under 510(k) number K870615.

Who is the listed applicant for VAN-TEC POSITIVE OPEN SEGURA BASKET?

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 VAN-TEC POSITIVE OPEN SEGURA BASKET?

The FDA product code for VAN-TEC POSITIVE OPEN SEGURA BASKET 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.

K880096VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUPK880095BERGER PROSTATE CULTURE CYTOLOGY BRUSHK880098VAN-TEC AUTO BIOPSY NEEDLEK880099VAN-TEC BLADDER EVACUATORK880094VAN-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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