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FDA 510(k)

FIRST CHOICE & FIRST CHOICE PLUS

K-Number: K022076 · 2002-09-24

ApplicantBody Clock Health Care, Ltd.
Decision Date2002-09-24
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FIRST CHOICE & FIRST CHOICE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Body Clock Health Care, Ltd.. It received FDA 510(k) clearance on 2002-09-24 under 510(k) number K022076. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST CHOICE & FIRST CHOICE PLUS?

FIRST CHOICE & FIRST CHOICE PLUS is a medical device that received FDA 510(k) clearance on 2002-09-24. The listed applicant is Body Clock Health Care, Ltd.. The 510(k) number is K022076.

When did FIRST CHOICE & FIRST CHOICE PLUS receive FDA 510(k) clearance?

FIRST CHOICE & FIRST CHOICE PLUS received FDA 510(k) clearance on 2002-09-24, under 510(k) number K022076.

Who is the listed applicant for FIRST CHOICE & FIRST CHOICE PLUS?

The FDA 510(k) record lists Body Clock Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIRST CHOICE & FIRST CHOICE PLUS?

The FDA product code for FIRST CHOICE & FIRST CHOICE PLUS is GZJ.

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Other records listing Body Clock Health Care, Ltd. 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.

K091045SMART TENS, MODEL: D-BC05TK041359BODY CLOCK STIMPLUS AND STIMPLUS PROK022849BODY CLOCK TENS N' TONEK021846804SIII; 804W; LIBRA TENS; 410; S-TENS IIK022731V TENS PLUSK022493EMS 400

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Related Devices (Code: GZJ)

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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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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