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)

ELVAREX

K-Number: K963573 · 1996-10-16

Decision Date1996-10-16
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELVAREX is the device name listed in this FDA 510(k) record. The listed applicant is Jobst A Beiersdorf Co.. It received FDA 510(k) clearance on 1996-10-16 under 510(k) number K963573. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVAREX?

ELVAREX is a medical device that received FDA 510(k) clearance on 1996-10-16. The listed applicant is Jobst A Beiersdorf Co.. The 510(k) number is K963573.

When did ELVAREX receive FDA 510(k) clearance?

ELVAREX received FDA 510(k) clearance on 1996-10-16, under 510(k) number K963573.

Who is the listed applicant for ELVAREX?

The FDA 510(k) record lists Jobst A Beiersdorf Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELVAREX?

The FDA product code for ELVAREX is DWL.

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 Jobst A Beiersdorf Co. 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: DWL)

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.

↑