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FDA 510(k)

RELIANCE LIGHT CURE RETAINER ACRYLIC

K-Number: K894564 · 1989-10-17

ApplicantReliance Orthodontic Products, Inc.
Decision Date1989-10-17
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RELIANCE LIGHT CURE RETAINER ACRYLIC is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Orthodontic Products, Inc.. It received FDA 510(k) clearance on 1989-10-17 under 510(k) number K894564. 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 RELIANCE LIGHT CURE RETAINER ACRYLIC?

RELIANCE LIGHT CURE RETAINER ACRYLIC is a medical device that received FDA 510(k) clearance on 1989-10-17. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K894564.

When did RELIANCE LIGHT CURE RETAINER ACRYLIC receive FDA 510(k) clearance?

RELIANCE LIGHT CURE RETAINER ACRYLIC received FDA 510(k) clearance on 1989-10-17, under 510(k) number K894564.

Who is the listed applicant for RELIANCE LIGHT CURE RETAINER ACRYLIC?

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

What is the FDA product code for RELIANCE LIGHT CURE RETAINER ACRYLIC?

The FDA product code for RELIANCE LIGHT CURE RETAINER ACRYLIC is EBI.

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Related Devices (Code: EBI)

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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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