RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX
K-Number: K862613 · 1986-11-10
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Device Summary
Frequently Asked Questions
What is the RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX?
RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX is a medical device that received FDA 510(k) clearance on 1986-11-10. The listed applicant is Gen-Probe, Inc.. The 510(k) number is K862613.
When did RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX receive FDA 510(k) clearance?
RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX received FDA 510(k) clearance on 1986-11-10, under 510(k) number K862613.
Who is the listed applicant for RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX?
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 RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX?
The FDA product code for RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX is LQF.
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: LQF)
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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