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)

RHIGENE MESACUP2 TEST- SSB

K-Number: K000751 · 2000-05-09

ApplicantRhigene, Inc.
Decision Date2000-05-09
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

RHIGENE MESACUP2 TEST- SSB is the device name listed in this FDA 510(k) record. The listed applicant is Rhigene, Inc.. It received FDA 510(k) clearance on 2000-05-09 under 510(k) number K000751. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHIGENE MESACUP2 TEST- SSB?

RHIGENE MESACUP2 TEST- SSB is a medical device that received FDA 510(k) clearance on 2000-05-09. The listed applicant is Rhigene, Inc.. The 510(k) number is K000751.

When did RHIGENE MESACUP2 TEST- SSB receive FDA 510(k) clearance?

RHIGENE MESACUP2 TEST- SSB received FDA 510(k) clearance on 2000-05-09, under 510(k) number K000751.

Who is the listed applicant for RHIGENE MESACUP2 TEST- SSB?

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

What is the FDA product code for RHIGENE MESACUP2 TEST- SSB?

The FDA product code for RHIGENE MESACUP2 TEST- SSB is LLL.

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 Rhigene, 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.

View all 15 devices →

Related Devices (Code: LLL)

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.

↑