ELVAREX
K-Number: K963573 · 1996-10-16
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Device Summary
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.
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