HELICAL STONE BASKET (DISPOSABLE)
K-Number: K871779 · 1987-06-17
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Device Summary
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.
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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