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FDA 510(k)

MIRAGE BOND

K-Number: K884137 · 1988-12-07

ApplicantChameleon Dental Products, Inc.
Decision Date1988-12-07
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIRAGE BOND is the device name listed in this FDA 510(k) record. The listed applicant is Chameleon Dental Products, Inc.. It received FDA 510(k) clearance on 1988-12-07 under 510(k) number K884137. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIRAGE BOND?

MIRAGE BOND is a medical device that received FDA 510(k) clearance on 1988-12-07. The listed applicant is Chameleon Dental Products, Inc.. The 510(k) number is K884137.

When did MIRAGE BOND receive FDA 510(k) clearance?

MIRAGE BOND received FDA 510(k) clearance on 1988-12-07, under 510(k) number K884137.

Who is the listed applicant for MIRAGE BOND?

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

What is the FDA product code for MIRAGE BOND?

The FDA product code for MIRAGE BOND is KLE.

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Related Devices (Code: KLE)

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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