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FDA 510(k)

SSIR SYSTEM

K-Number: K014208 · 2002-07-02

ApplicantRussian-American Technology Associates, Inc.
Decision Date2002-07-02
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SSIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Russian-American Technology Associates, Inc.. It received FDA 510(k) clearance on 2002-07-02 under 510(k) number K014208. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSIR SYSTEM?

SSIR SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-02. The listed applicant is Russian-American Technology Associates, Inc.. The 510(k) number is K014208.

When did SSIR SYSTEM receive FDA 510(k) clearance?

SSIR SYSTEM received FDA 510(k) clearance on 2002-07-02, under 510(k) number K014208.

Who is the listed applicant for SSIR SYSTEM?

The FDA 510(k) record lists Russian-American Technology Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SSIR SYSTEM?

The FDA product code for SSIR SYSTEM is ILY.

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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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