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FDA 510(k)

BISCOVER LED

K-Number: K051999 · 2005-08-22

ApplicantBisco, Inc.
Decision Date2005-08-22
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BISCOVER LED is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 2005-08-22 under 510(k) number K051999. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BISCOVER LED?

BISCOVER LED is a medical device that received FDA 510(k) clearance on 2005-08-22. The listed applicant is Bisco, Inc.. The 510(k) number is K051999.

When did BISCOVER LED receive FDA 510(k) clearance?

BISCOVER LED received FDA 510(k) clearance on 2005-08-22, under 510(k) number K051999.

Who is the listed applicant for BISCOVER LED?

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

What is the FDA product code for BISCOVER LED?

The FDA product code for BISCOVER LED is EBD.

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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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