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FDA 510(k)

YORAMED, MODEL T-202

K-Number: K002297 · 2001-03-15

ApplicantUnited Yoram Distributors, Inc.
Decision Date2001-03-15
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

YORAMED, MODEL T-202 is the device name listed in this FDA 510(k) record. The listed applicant is United Yoram Distributors, Inc.. It received FDA 510(k) clearance on 2001-03-15 under 510(k) number K002297. 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 YORAMED, MODEL T-202?

YORAMED, MODEL T-202 is a medical device that received FDA 510(k) clearance on 2001-03-15. The listed applicant is United Yoram Distributors, Inc.. The 510(k) number is K002297.

When did YORAMED, MODEL T-202 receive FDA 510(k) clearance?

YORAMED, MODEL T-202 received FDA 510(k) clearance on 2001-03-15, under 510(k) number K002297.

Who is the listed applicant for YORAMED, MODEL T-202?

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

What is the FDA product code for YORAMED, MODEL T-202?

The FDA product code for YORAMED, MODEL T-202 is GZJ.

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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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