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FDA 510(k)

MICROARCH GOLD BRACKET

K-Number: K932825 · 1994-05-09

ApplicantGac Intl., Inc.
Decision Date1994-05-09
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROARCH GOLD BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Gac Intl., Inc.. It received FDA 510(k) clearance on 1994-05-09 under 510(k) number K932825. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROARCH GOLD BRACKET?

MICROARCH GOLD BRACKET is a medical device that received FDA 510(k) clearance on 1994-05-09. The listed applicant is Gac Intl., Inc.. The 510(k) number is K932825.

When did MICROARCH GOLD BRACKET receive FDA 510(k) clearance?

MICROARCH GOLD BRACKET received FDA 510(k) clearance on 1994-05-09, under 510(k) number K932825.

Who is the listed applicant for MICROARCH GOLD BRACKET?

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

What is the FDA product code for MICROARCH GOLD BRACKET?

The FDA product code for MICROARCH GOLD BRACKET is EJF.

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Other records listing Gac Intl., 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.

K981036SMARTBONDK942826ORTHODONITC METAL REINFORCED PLASTIC BRACKETK933542MESIAL LOOP BARK932319ORTHODONTIC ELASTOMERK932025ION-IMPLANTED NEO SENTALLOYK920905BIOFORCE WIRE

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Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.K936244REGENCY BRACKETMid-American Dental Specialties, Inc.

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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