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FDA 510(k)

AB BELT

K-Number: K020427 · 2002-09-13

ApplicantThe Dezac Group
Decision Date2002-09-13
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AB BELT is the device name listed in this FDA 510(k) record. The listed applicant is The Dezac Group. It received FDA 510(k) clearance on 2002-09-13 under 510(k) number K020427. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AB BELT?

AB BELT is a medical device that received FDA 510(k) clearance on 2002-09-13. The listed applicant is The Dezac Group. The 510(k) number is K020427.

When did AB BELT receive FDA 510(k) clearance?

AB BELT received FDA 510(k) clearance on 2002-09-13, under 510(k) number K020427.

Who is the listed applicant for AB BELT?

The FDA 510(k) record lists The Dezac Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AB BELT?

The FDA product code for AB BELT is NGX.

Other records listing The Dezac Group 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.

K020429AB BELT PROK022006CONDUCTIVE GEL

Related Devices (Code: NGX)

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.

K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)Beijing Winkonlaser Technology LimitedK253926DiacoreShenB Co., Ltd.K253636Zionic Pro Max (EMS)Termosalud S.L.K253408CoolToneZimmer Medizinsysteme GmbHK252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)Guangzhou Longest Medical Technology Co., Ltd.K253478Motive™ Muscle Stimulator for Lower Back (OT01-1003)Motive Health, Inc.

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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