LEGIONELLA INDIRECT FLUOR. ANTIBODY
K-Number: K812007 · 1981-09-08
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Device Summary
Frequently Asked Questions
What is the LEGIONELLA INDIRECT FLUOR. ANTIBODY?
LEGIONELLA INDIRECT FLUOR. ANTIBODY is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Centers for Disease Control and Prevention. The 510(k) number is K812007.
When did LEGIONELLA INDIRECT FLUOR. ANTIBODY receive FDA 510(k) clearance?
LEGIONELLA INDIRECT FLUOR. ANTIBODY received FDA 510(k) clearance on 1981-09-08, under 510(k) number K812007.
Who is the listed applicant for LEGIONELLA INDIRECT FLUOR. ANTIBODY?
The FDA 510(k) record lists Centers for Disease Control and Prevention as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEGIONELLA INDIRECT FLUOR. ANTIBODY?
The FDA product code for LEGIONELLA INDIRECT FLUOR. ANTIBODY is LHL.
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 Centers for Disease Control and Prevention 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: LHL)
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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