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FDA 510(k)

PORTABLE LIGHT CURING UNIT

K-Number: K994048 · 2000-01-13

ApplicantGregory S. Jacob, D.D.S.
Decision Date2000-01-13
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORTABLE LIGHT CURING UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Gregory S. Jacob, D.D.S.. It received FDA 510(k) clearance on 2000-01-13 under 510(k) number K994048. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE LIGHT CURING UNIT?

PORTABLE LIGHT CURING UNIT is a medical device that received FDA 510(k) clearance on 2000-01-13. The listed applicant is Gregory S. Jacob, D.D.S.. The 510(k) number is K994048.

When did PORTABLE LIGHT CURING UNIT receive FDA 510(k) clearance?

PORTABLE LIGHT CURING UNIT received FDA 510(k) clearance on 2000-01-13, under 510(k) number K994048.

Who is the listed applicant for PORTABLE LIGHT CURING UNIT?

The FDA 510(k) record lists Gregory S. Jacob, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE LIGHT CURING UNIT?

The FDA product code for PORTABLE LIGHT CURING UNIT is EBZ.

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Related Devices (Code: EBZ)

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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