Emit and Netilmicin Assay

FDA 510(k) K820324 · Syva Co.

Substantially Equivalent

510(k) numberK820324

Submission

Device name
Emit and Netilmicin Assay
Applicant
Syva Co.
Mchenry, IL, US
Received
February 5, 1982
Decision date
February 23, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCE – Radioimmunoassay, Netilmicin (I-125)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3450
Specialty
Clinical Toxicology

Other 510(k)s with product code LCE

510(k)DeviceApplicantDecision
K833715Emit Netilmicin AssayLCE · Traditional Syva Co.12/27/1983SE
K832088Ames Tda Netilmicin Test & SerumLCE · Traditional Miles Laboratories, Inc.10/28/1983SE
K822941Netilmicin Fluorescent ImmunoassayLCE · Traditional American Diagnostic Corp.10/26/1982SE
K821698TDX NetilmicinLCE · Traditional Abbott Laboratories06/22/1982SE
K821399Macro-Vue Card Test, NetilmicinLCE · Traditional Bd Becton Dickinson Vacutainer Systems Preanalytic05/28/1982SE

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Questions and answers

When was Emit and Netilmicin Assay cleared by the FDA?

Emit and Netilmicin Assay (K820324) received a 510(k) decision of Substantially Equivalent on February 23, 1982, 18 days after the submission was received.

What is the product code of K820324?

The FDA product code is LCE – Radioimmunoassay, Netilmicin (I-125), a Class II (moderate risk) device regulated under 21 CFR 862.3450.