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)

RHODIA BITE REGISTRATION MATERIAL

K-Number: K013859 · 2002-01-29

ApplicantRhodia, Inc.
Decision Date2002-01-29
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RHODIA BITE REGISTRATION MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Rhodia, Inc.. It received FDA 510(k) clearance on 2002-01-29 under 510(k) number K013859. 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 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.

↑