GEN-PROBE (R) LUMINOMETER - LEADER (TM)
K-Number: K872219 · 1987-08-21
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Device Summary
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.
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.
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