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FDA 510(k)

INSTANT CURE-1

K-Number: K780898 · 1978-06-30

ApplicantUltra-Light Corp.
Decision Date1978-06-30
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INSTANT CURE-1 is the device name listed in this FDA 510(k) record. The listed applicant is Ultra-Light Corp.. It received FDA 510(k) clearance on 1978-06-30 under 510(k) number K780898. 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 INSTANT CURE-1?

INSTANT CURE-1 is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Ultra-Light Corp.. The 510(k) number is K780898.

When did INSTANT CURE-1 receive FDA 510(k) clearance?

INSTANT CURE-1 received FDA 510(k) clearance on 1978-06-30, under 510(k) number K780898.

Who is the listed applicant for INSTANT CURE-1?

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

What is the FDA product code for INSTANT CURE-1?

The FDA product code for INSTANT CURE-1 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.

K253131Curing Light (M-Cure 6)Guangzhou Rebornendo Medical Instrument Co., Ltd.K253461Demi ProMeta Systems Co., Ltd.K242386BluemoonGenoss Co., Ltd.K243921LED Curing Lights (DB686 HALO)Foshan Coxo Medical Instrument Co., Ltd.K250009LED Curing Light (C01-X, C02-X)Premium Plus (Dongguan) LimitedK241238LOOP™ LED Curing Light System (CLK01)Garrison Dental Solutions, LLC

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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