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FDA 510(k)

SLIMMANAGER, MODEL SM-X, SM-E

K-Number: K051589 · 2005-10-31

ApplicantAiia Communication, Inc.
Decision Date2005-10-31
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SLIMMANAGER, MODEL SM-X, SM-E is the device name listed in this FDA 510(k) record. The listed applicant is Aiia Communication, Inc.. It received FDA 510(k) clearance on 2005-10-31 under 510(k) number K051589. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIMMANAGER, MODEL SM-X, SM-E?

SLIMMANAGER, MODEL SM-X, SM-E is a medical device that received FDA 510(k) clearance on 2005-10-31. The listed applicant is Aiia Communication, Inc.. The 510(k) number is K051589.

When did SLIMMANAGER, MODEL SM-X, SM-E receive FDA 510(k) clearance?

SLIMMANAGER, MODEL SM-X, SM-E received FDA 510(k) clearance on 2005-10-31, under 510(k) number K051589.

Who is the listed applicant for SLIMMANAGER, MODEL SM-X, SM-E?

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

What is the FDA product code for SLIMMANAGER, MODEL SM-X, SM-E?

The FDA product code for SLIMMANAGER, MODEL SM-X, SM-E is MNW.

Related Clinical Trials

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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Other records listing Aiia Communication, 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.

K073227SLIMMANAGER BODY COMPOSITION ANALYZER, MODELS N40 AND SM-300

Related Devices (Code: MNW)

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.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.

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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