Syva(R) Ets(R) Plus System

FDA 510(k) K903357 · Syva Co.

Substantially Equivalent

510(k) numberK903357

Submission

Device name
Syva(R) Ets(R) Plus System
Applicant
Syva Co.
Palo Alto, CA, US
Received
July 26, 1990
Decision date
September 27, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJF – Analyzer, Chemistry, Micro, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2170
Specialty
Clinical Chemistry

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K993980Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULDML · Traditional 02/01/2000SE
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Questions and answers

When was Syva(R) Ets(R) Plus System cleared by the FDA?

Syva(R) Ets(R) Plus System (K903357) received a 510(k) decision of Substantially Equivalent on September 27, 1990, 63 days after the submission was received.

What is the product code of K903357?

The FDA product code is JJF – Analyzer, Chemistry, Micro, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2170.