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FDA 510(k)

HELICAL STONE BASKET (DISPOSABLE)

K-Number: K871779 · 1987-06-17

ApplicantVan-Tec, Inc.
Decision Date1987-06-17
Product CodeFFL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HELICAL STONE BASKET (DISPOSABLE) 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 1987-06-17 under 510(k) number K871779. 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 HELICAL STONE BASKET (DISPOSABLE)?

HELICAL STONE BASKET (DISPOSABLE) is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is Van-Tec, Inc.. The 510(k) number is K871779.

When did HELICAL STONE BASKET (DISPOSABLE) receive FDA 510(k) clearance?

HELICAL STONE BASKET (DISPOSABLE) received FDA 510(k) clearance on 1987-06-17, under 510(k) number K871779.

Who is the listed applicant for HELICAL STONE BASKET (DISPOSABLE)?

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 HELICAL STONE BASKET (DISPOSABLE)?

The FDA product code for HELICAL STONE BASKET (DISPOSABLE) 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.

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.

View all 52 devices →

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.

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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