Emit Convenience Pack: Tobramycin Assay

FDA 510(k) K882294 · Syva Co.

Substantially Equivalent

510(k) numberK882294

Submission

Device name
Emit Convenience Pack: Tobramycin Assay
Applicant
Syva Co.
Palo Alto, CA, US
Received
June 2, 1988
Decision date
July 1, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KLB – Radioimmunoassay, Tobramycin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3900
Specialty
Clinical Toxicology

Other 510(k)s with product code KLB

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K060853Online TDM TobramycinKLB · Traditional Roche Diagnostics Corp.06/09/2006SE
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K003341Emit 2000 Tobramycin Assay Emit 2000 Tobramycin CalibratorsKLB · Traditional Syva Co., Dade Behring, Inc.01/22/2001SE
K904304Dupont Dimension(R) Tobramllycin(Tobr) MethodKLB · Traditional E.I. Dupont DE Nemours & Co., Inc.10/26/1990SE
K903192Il Tobramycin AssayKLB · Traditional Instrumentation Laboratory CO08/22/1990SE
K893913Technicon Ra Systems Tobramycin Test MethodKLB · Traditional Technicon Instruments Corp.08/21/1989SE
K874223Emit Tobramycin AssayKLB · Traditional Syva Co.11/13/1987SE
K854184In-Vitro Test Determination of TobramycinKLB · Traditional Clinical Data, Inc.12/04/1985SE
K852671Aca Tobramy-Cin Analytical Test PackKLB · Traditional E.I. Dupont DE Nemours & Co., Inc.07/22/1985SE
K832763Tobramycin ReagentKLB · Traditional Biosan Laboratories, Inc.03/23/1984SE

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Questions and answers

When was Emit Convenience Pack: Tobramycin Assay cleared by the FDA?

Emit Convenience Pack: Tobramycin Assay (K882294) received a 510(k) decision of Substantially Equivalent on July 1, 1988, 29 days after the submission was received.

What is the product code of K882294?

The FDA product code is KLB – Radioimmunoassay, Tobramycin, a Class II (moderate risk) device regulated under 21 CFR 862.3900.