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FDA 510(k)

TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4.

K-Number: K992310 · 1999-11-02

ApplicantRupiani Medical
Decision Date1999-11-02
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4. is the device name listed in this FDA 510(k) record. The listed applicant is Rupiani Medical. It received FDA 510(k) clearance on 1999-11-02 under 510(k) number K992310. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4.?

TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4. is a medical device that received FDA 510(k) clearance on 1999-11-02. The listed applicant is Rupiani Medical. The 510(k) number is K992310.

When did TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4. receive FDA 510(k) clearance?

TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4. received FDA 510(k) clearance on 1999-11-02, under 510(k) number K992310.

Who is the listed applicant for TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4.?

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

What is the FDA product code for TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4.?

The FDA product code for TONICROSS TRICYCLES, MODELS, T0, T1,T2,T3 AND T4. is IOR.

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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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