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FDA 510(k)

MAR BOND

K-Number: K875145 · 1988-02-26

Decision Date1988-02-26
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAR BOND 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 1988-02-26 under 510(k) number K875145. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAR BOND?

MAR BOND is a medical device that received FDA 510(k) clearance on 1988-02-26. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K875145.

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

MAR BOND received FDA 510(k) clearance on 1988-02-26, under 510(k) number K875145.

Who is the listed applicant for MAR BOND?

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 MAR BOND?

The FDA product code for MAR BOND is EBG.

Other records listing Reliance Orthodontic Products, Inc. as applicant

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.

View all 32 devices →

Related Devices (Code: EBG)

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.

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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