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FDA 510(k)

MIRACLE MIX CAPSULE

K-Number: K981370 · 1998-06-01

ApplicantGC America, Inc.
Decision Date1998-06-01
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIRACLE MIX CAPSULE is the device name listed in this FDA 510(k) record. The listed applicant is GC America, Inc.. It received FDA 510(k) clearance on 1998-06-01 under 510(k) number K981370. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIRACLE MIX CAPSULE?

MIRACLE MIX CAPSULE is a medical device that received FDA 510(k) clearance on 1998-06-01. The listed applicant is GC America, Inc.. The 510(k) number is K981370.

When did MIRACLE MIX CAPSULE receive FDA 510(k) clearance?

MIRACLE MIX CAPSULE received FDA 510(k) clearance on 1998-06-01, under 510(k) number K981370.

Who is the listed applicant for MIRACLE MIX CAPSULE?

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

What is the FDA product code for MIRACLE MIX CAPSULE?

The FDA product code for MIRACLE MIX CAPSULE is EMA.

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Other records listing GC America, Inc. as applicant

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Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, 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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