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FDA 510(k)

JBC OPAQUE AND GLITTER

K-Number: K002048 · 2000-08-30

ApplicantJ.B.C and Co.
Decision Date2000-08-30
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JBC OPAQUE AND GLITTER is the device name listed in this FDA 510(k) record. The listed applicant is J.B.C and Co.. It received FDA 510(k) clearance on 2000-08-30 under 510(k) number K002048. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JBC OPAQUE AND GLITTER?

JBC OPAQUE AND GLITTER is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is J.B.C and Co.. The 510(k) number is K002048.

When did JBC OPAQUE AND GLITTER receive FDA 510(k) clearance?

JBC OPAQUE AND GLITTER received FDA 510(k) clearance on 2000-08-30, under 510(k) number K002048.

Who is the listed applicant for JBC OPAQUE AND GLITTER?

The FDA 510(k) record lists J.B.C and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JBC OPAQUE AND GLITTER?

The FDA product code for JBC OPAQUE AND GLITTER is EBI.

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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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