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FDA 510(k)

WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT

K-Number: K895085 · 1990-04-02

ApplicantLustgarten Multi-Tech International, Inc.
Decision Date1990-04-02
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Lustgarten Multi-Tech International, Inc.. It received FDA 510(k) clearance on 1990-04-02 under 510(k) number K895085. 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 WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT?

WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is Lustgarten Multi-Tech International, Inc.. The 510(k) number is K895085.

When did WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT receive FDA 510(k) clearance?

WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT received FDA 510(k) clearance on 1990-04-02, under 510(k) number K895085.

Who is the listed applicant for WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT?

The FDA 510(k) record lists Lustgarten Multi-Tech International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT?

The FDA product code for WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT is EBZ.

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Other records listing Lustgarten Multi-Tech International, Inc. as applicant

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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

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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