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)

MP RAPIDOXY TEST STRIP, MODEL 07RD-7073

K-Number: K051958 · 2006-07-21

Decision Date2006-07-21
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MP RAPIDOXY TEST STRIP, MODEL 07RD-7073 is the device name listed in this FDA 510(k) record. The listed applicant is Mp Biomedicals, LLC. It received FDA 510(k) clearance on 2006-07-21 under 510(k) number K051958. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MP RAPIDOXY TEST STRIP, MODEL 07RD-7073?

MP RAPIDOXY TEST STRIP, MODEL 07RD-7073 is a medical device that received FDA 510(k) clearance on 2006-07-21. The listed applicant is Mp Biomedicals, LLC. The 510(k) number is K051958.

When did MP RAPIDOXY TEST STRIP, MODEL 07RD-7073 receive FDA 510(k) clearance?

MP RAPIDOXY TEST STRIP, MODEL 07RD-7073 received FDA 510(k) clearance on 2006-07-21, under 510(k) number K051958.

Who is the listed applicant for MP RAPIDOXY TEST STRIP, MODEL 07RD-7073?

The FDA 510(k) record lists Mp Biomedicals, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MP RAPIDOXY TEST STRIP, MODEL 07RD-7073?

The FDA product code for MP RAPIDOXY TEST STRIP, MODEL 07RD-7073 is DJG.

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 Mp Biomedicals, LLC 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: DJG)

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.

↑