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FDA 510(k)

MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02

K-Number: K023293 · 2002-12-23

ApplicantMed-Tec,Inc.
Decision Date2002-12-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02 is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tec,Inc.. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K023293. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02?

MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02 is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Med-Tec,Inc.. The 510(k) number is K023293.

When did MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02 receive FDA 510(k) clearance?

MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02 received FDA 510(k) clearance on 2002-12-23, under 510(k) number K023293.

Who is the listed applicant for MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02?

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

What is the FDA product code for MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02?

The FDA product code for MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02 is IYE.

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Other records listing Med-Tec,Inc. as applicant

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Related Devices (Code: IYE)

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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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