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)

ZETAPLUS SOFT

K-Number: K024041 · 2002-12-18

Decision Date2002-12-18
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZETAPLUS SOFT is the device name listed in this FDA 510(k) record. The listed applicant is Zhermack S.P.A.. It received FDA 510(k) clearance on 2002-12-18 under 510(k) number K024041. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZETAPLUS SOFT?

ZETAPLUS SOFT is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Zhermack S.P.A.. The 510(k) number is K024041.

When did ZETAPLUS SOFT receive FDA 510(k) clearance?

ZETAPLUS SOFT received FDA 510(k) clearance on 2002-12-18, under 510(k) number K024041.

Who is the listed applicant for ZETAPLUS SOFT?

The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZETAPLUS SOFT?

The FDA product code for ZETAPLUS SOFT is ELW.

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 Zhermack S.P.A. 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 19 devices →

Related Devices (Code: ELW)

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.

↑