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FDA 510(k)

RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,

K-Number: K032402 · 2003-09-24

ApplicantConvaid Products, Inc.
Decision Date2003-09-24
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T, is the device name listed in this FDA 510(k) record. The listed applicant is Convaid Products, Inc.. It received FDA 510(k) clearance on 2003-09-24 under 510(k) number K032402. 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 RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,?

RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T, is a medical device that received FDA 510(k) clearance on 2003-09-24. The listed applicant is Convaid Products, Inc.. The 510(k) number is K032402.

When did RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T, receive FDA 510(k) clearance?

RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T, received FDA 510(k) clearance on 2003-09-24, under 510(k) number K032402.

Who is the listed applicant for RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,?

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

What is the FDA product code for RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,?

The FDA product code for RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T, is IOR.

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Other records listing Convaid Products, Inc. as applicant

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Related Devices (Code: IOR)

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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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