RHODIA BITE REGISTRATION MATERIAL
K-Number: K013859 · 2002-01-29
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Device Summary
Frequently Asked Questions
What is the RHODIA BITE REGISTRATION MATERIAL?
RHODIA BITE REGISTRATION MATERIAL is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is Rhodia, Inc.. The 510(k) number is K013859.
When did RHODIA BITE REGISTRATION MATERIAL receive FDA 510(k) clearance?
RHODIA BITE REGISTRATION MATERIAL received FDA 510(k) clearance on 2002-01-29, under 510(k) number K013859.
Who is the listed applicant for RHODIA BITE REGISTRATION MATERIAL?
The FDA 510(k) record lists Rhodia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RHODIA BITE REGISTRATION MATERIAL?
The FDA product code for RHODIA BITE REGISTRATION MATERIAL 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 Rhodia, Inc. 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: 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.
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