Emds TM Phenobarbital(Phno) Testpack, #67677/95

FDA 510(k) K864926 · Em Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK864926

Submission

Device name
Emds TM Phenobarbital(Phno) Testpack, #67677/95
Applicant
Em Diagnostic Systems, Inc.
Gibbstown, NJ, US
Received
December 16, 1986
Decision date
January 7, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DLZ – Enzyme Immunoassay, Phenobarbital
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3660
Specialty
Clinical Toxicology

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K946210Phenobarbital Enzyme ImmunoassayDLZ · Traditional Diagnostic Reagents, Inc.02/10/1995SE

More from Diagnostic Reagents, Inc.

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K935179Emds Albumin (Alb) TestCIX · Traditional 12/17/1993SE
K935178Emds Phosphorous (Phos) TestCEO · Traditional 12/17/1993SE
K935177Gamma-Glutamyl Transferase (GGT) TestJQB · Traditional 12/16/1993SE
K935176Iron TestJIY · Traditional 12/16/1993SE
K935175Lactate Dehydrogenase (LD)CFJ · Traditional 12/16/1993SE
K935174Total Protein Test (Tpro)CEK · Traditional 12/16/1993SE
K935136Cholesterol (Chol) Test Item No. 65410CHH · Traditional 12/16/1993SE
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Questions and answers

When was Emds TM Phenobarbital(Phno) Testpack, #67677/95 cleared by the FDA?

Emds TM Phenobarbital(Phno) Testpack, #67677/95 (K864926) received a 510(k) decision of Substantially Equivalent on January 7, 1987, 22 days after the submission was received.

What is the product code of K864926?

The FDA product code is DLZ – Enzyme Immunoassay, Phenobarbital, a Class II (moderate risk) device regulated under 21 CFR 862.3660.