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FDA 510(k)

CHAMP CHAMP TRANSIT

K-Number: K120501 · 2012-09-20

Decision Date2012-09-20
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHAMP CHAMP TRANSIT 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 2012-09-20 under 510(k) number K120501. 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 CHAMP CHAMP TRANSIT?

CHAMP CHAMP TRANSIT is a medical device that received FDA 510(k) clearance on 2012-09-20. The listed applicant is Convaid Products, Inc.. The 510(k) number is K120501.

When did CHAMP CHAMP TRANSIT receive FDA 510(k) clearance?

CHAMP CHAMP TRANSIT received FDA 510(k) clearance on 2012-09-20, under 510(k) number K120501.

Who is the listed applicant for CHAMP CHAMP TRANSIT?

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 CHAMP CHAMP TRANSIT?

The FDA product code for CHAMP CHAMP TRANSIT is IOR.

Related Clinical Trials

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.

Other records listing Convaid Products, Inc. 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.

View all 7 devices →

Related Devices (Code: IOR)

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.

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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