Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Single-use Extraction Baskets

K-Number: K240192 · 2024-10-15

Decision Date2024-10-15
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single-use Extraction Baskets is the device name listed in this FDA 510(k) record. The listed applicant is Scivita Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-10-15 under 510(k) number K240192. 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 Single-use Extraction Baskets?

Single-use Extraction Baskets is a medical device that received FDA 510(k) clearance on 2024-10-15. The listed applicant is Scivita Medical Technology Co., Ltd.. The 510(k) number is K240192.

When did Single-use Extraction Baskets receive FDA 510(k) clearance?

Single-use Extraction Baskets received FDA 510(k) clearance on 2024-10-15, under 510(k) number K240192.

Who is the listed applicant for Single-use Extraction Baskets?

The FDA 510(k) record lists Scivita Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Single-use Extraction Baskets?

The FDA product code for Single-use Extraction Baskets is LQR.

Other records listing Scivita Medical Technology Co., Ltd. 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 13 devices →

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.

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.