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FDA 510(k)

SEGURA DRETLER BASKET

K-Number: K864874 · 1987-03-10

ApplicantVan-Tec, Inc.
Decision Date1987-03-10
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SEGURA DRETLER 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 1987-03-10 under 510(k) number K864874. 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 SEGURA DRETLER BASKET?

SEGURA DRETLER BASKET is a medical device that received FDA 510(k) clearance on 1987-03-10. The listed applicant is Van-Tec, Inc.. The 510(k) number is K864874.

When did SEGURA DRETLER BASKET receive FDA 510(k) clearance?

SEGURA DRETLER BASKET received FDA 510(k) clearance on 1987-03-10, under 510(k) number K864874.

Who is the listed applicant for SEGURA DRETLER 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 SEGURA DRETLER BASKET?

The FDA product code for SEGURA DRETLER BASKET is FFL.

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Other records listing Van-Tec, Inc. as applicant

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Related Devices (Code: FFL)

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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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