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)

GEN-PROBE (R) LUMINOMETER - LEADER (TM)

K-Number: K872219 · 1987-08-21

Decision Date1987-08-21
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GEN-PROBE (R) LUMINOMETER - LEADER (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Gen-Probe, Inc.. It received FDA 510(k) clearance on 1987-08-21 under 510(k) number K872219. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GEN-PROBE (R) LUMINOMETER - LEADER (TM)?

GEN-PROBE (R) LUMINOMETER - LEADER (TM) is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Gen-Probe, Inc.. The 510(k) number is K872219.

When did GEN-PROBE (R) LUMINOMETER - LEADER (TM) receive FDA 510(k) clearance?

GEN-PROBE (R) LUMINOMETER - LEADER (TM) received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872219.

Who is the listed applicant for GEN-PROBE (R) LUMINOMETER - LEADER (TM)?

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

What is the FDA product code for GEN-PROBE (R) LUMINOMETER - LEADER (TM)?

The FDA product code for GEN-PROBE (R) LUMINOMETER - LEADER (TM) is JJQ.

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 Gen-Probe, 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 62 devices →

Related Devices (Code: JJQ)

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.

↑