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FDA 510(k)

RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX

K-Number: K862613 · 1986-11-10

Decision Date1986-11-10
Product CodeLQF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RAPID IDENT. TEST FOR MYCOBACTERIUM AVIUM COMPLEX 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 1986-11-10 under 510(k) number K862613. The device is classified under product code LQF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 62 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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