Coat-A-Count(Tm) LSD Radioimmunoassay Kit

FDA 510(k) K891167 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK891167

Submission

Device name
Coat-A-Count(Tm) LSD Radioimmunoassay Kit
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
March 6, 1989
Decision date
May 3, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DLB – Radioimmunoassay, Lsd (125-I)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3580
Specialty
Clinical Toxicology

Other 510(k)s with product code DLB

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K961436Abuscreen Online LSD Reagent (90 ML Test Kit)DLB · Traditional Roche Diagnostic Systems, Inc.06/21/1996SE
K955448Emit II LSD Assay, Emit LSD Calibrators & Emit LSD ControlsDLB · Traditional Behring Diagnostics, Inc.02/23/1996SE
K955814Cedia Dau LSD AssayDLB · Traditional Microgenics Corp.02/09/1996SE
K954073STC Diagnostics LSD Micro-Plate EiaDLB · Traditional Solarcare Technologies Corp,Inc.11/29/1995SE
K874270Revised Labeling for LSD Test KitDLB · Traditional Roche Diagnostic Systems, Inc.11/13/1987SE
K860525Abuscreen Radioimmunoassay for LSD W/ Ref StandardDLB · Traditional Roche Diagnostic Systems, Inc.04/11/1986SE

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Questions and answers

When was Coat-A-Count(Tm) LSD Radioimmunoassay Kit cleared by the FDA?

Coat-A-Count(Tm) LSD Radioimmunoassay Kit (K891167) received a 510(k) decision of Substantially Equivalent on May 3, 1989, 58 days after the submission was received.

What is the product code of K891167?

The FDA product code is DLB – Radioimmunoassay, Lsd (125-I), a Class II (moderate risk) device regulated under 21 CFR 862.3580.