Revised Labeling for Syva Propoxyphene Assays

FDA 510(k) K874200 · Syva Co.

Substantially Equivalent

510(k) numberK874200

Submission

Device name
Revised Labeling for Syva Propoxyphene Assays
Applicant
Syva Co.
Palo Alto, CA, US
Received
October 14, 1987
Decision date
October 28, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JXN – Enzyme Immunoassay, Propoxyphene
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3700
Specialty
Clinical Toxicology

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Questions and answers

When was Revised Labeling for Syva Propoxyphene Assays cleared by the FDA?

Revised Labeling for Syva Propoxyphene Assays (K874200) received a 510(k) decision of Substantially Equivalent on October 28, 1987, 14 days after the submission was received.

What is the product code of K874200?

The FDA product code is JXN – Enzyme Immunoassay, Propoxyphene, a Class II (moderate risk) device regulated under 21 CFR 862.3700.