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FDA 510(k)

Amethyst HP PTA OTW 0.035 Catheter

K-Number: K241040 · 2024-12-18

Decision Date2024-12-18
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Amethyst HP PTA OTW 0.035 Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Natec Medical , Ltd.. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K241040. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Amethyst HP PTA OTW 0.035 Catheter?

Amethyst HP PTA OTW 0.035 Catheter is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Natec Medical , Ltd.. The 510(k) number is K241040.

When did Amethyst HP PTA OTW 0.035 Catheter receive FDA 510(k) clearance?

Amethyst HP PTA OTW 0.035 Catheter received FDA 510(k) clearance on 2024-12-18, under 510(k) number K241040.

Who is the listed applicant for Amethyst HP PTA OTW 0.035 Catheter?

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

What is the FDA product code for Amethyst HP PTA OTW 0.035 Catheter?

The FDA product code for Amethyst HP PTA OTW 0.035 Catheter is LIT.

Other records listing Natec Medical , 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.

Related Devices (Code: LIT)

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

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