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FDA 510(k)

HELI-TECH RETRIEVAL BASKET

K-Number: K926040 · 1992-12-23

ApplicantCape Tech Medical Products
Decision Date1992-12-23
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HELI-TECH RETRIEVAL BASKET is the device name listed in this FDA 510(k) record. The listed applicant is Cape Tech Medical Products. It received FDA 510(k) clearance on 1992-12-23 under 510(k) number K926040. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HELI-TECH RETRIEVAL BASKET?

HELI-TECH RETRIEVAL BASKET is a medical device that received FDA 510(k) clearance on 1992-12-23. The listed applicant is Cape Tech Medical Products. The 510(k) number is K926040.

When did HELI-TECH RETRIEVAL BASKET receive FDA 510(k) clearance?

HELI-TECH RETRIEVAL BASKET received FDA 510(k) clearance on 1992-12-23, under 510(k) number K926040.

Who is the listed applicant for HELI-TECH RETRIEVAL BASKET?

The FDA 510(k) record lists Cape Tech Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HELI-TECH RETRIEVAL BASKET?

The FDA product code for HELI-TECH RETRIEVAL BASKET is LQR.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cape Tech Medical Products 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.

K926038FLEX-TECH BALLOON DILATORK926039GUIDE-TECH ENCAPSULATED GUIDEWIRE

Related Devices (Code: LQR)

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.

K253056Disposable Stone Extraction BasketZhejiang Soudon Medical Technology Co., Ltd.K243807Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432POlympus Medical Systems Corp.K243471Extraction BasketMicro-Tech (Nanjing) Co., Ltd.K240192Single-use Extraction BasketsScivita Medical Technology Co., Ltd.K230598Stone Extraction BasketsJiangsu Vedkang Medical Science and Technology Co., Ltd.K203322SpyGlass Discover Retrieval BasketBoston Scientific Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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