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FDA 510(k)

BILI BLUE F20T12/BBY AND F40T12/BBY

K-Number: K090192 · 2009-04-24

ApplicantInterlectric Corp.
Decision Date2009-04-24
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BILI BLUE F20T12/BBY AND F40T12/BBY is the device name listed in this FDA 510(k) record. The listed applicant is Interlectric Corp.. It received FDA 510(k) clearance on 2009-04-24 under 510(k) number K090192. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILI BLUE F20T12/BBY AND F40T12/BBY?

BILI BLUE F20T12/BBY AND F40T12/BBY is a medical device that received FDA 510(k) clearance on 2009-04-24. The listed applicant is Interlectric Corp.. The 510(k) number is K090192.

When did BILI BLUE F20T12/BBY AND F40T12/BBY receive FDA 510(k) clearance?

BILI BLUE F20T12/BBY AND F40T12/BBY received FDA 510(k) clearance on 2009-04-24, under 510(k) number K090192.

Who is the listed applicant for BILI BLUE F20T12/BBY AND F40T12/BBY?

The FDA 510(k) record lists Interlectric Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BILI BLUE F20T12/BBY AND F40T12/BBY?

The FDA product code for BILI BLUE F20T12/BBY AND F40T12/BBY is LBI.

Other records listing Interlectric Corp. 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.

K864907SUNTANNING LAMP

Related Devices (Code: LBI)

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.

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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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