Atomlight (Liquid Scintillation Solution

FDA 510(k) K801245 · New England Nuclear

Substantially Equivalent

510(k) numberK801245

Submission

Device name
Atomlight (Liquid Scintillation Solution
Applicant
New England Nuclear
Mchenry, IL, US
Received
May 27, 1980
Decision date
June 20, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJJ – Counter (Beta, Gamma) For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2320
Specialty
Clinical Chemistry

Other 510(k)s with product code JJJ

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K962762Sequential Sample Multi-Photon DetectorJJJ · Traditional Biotraces, Inc.08/16/1996SE
K946387Capra (Caprac-R) Wipetest and Well CounterJJJ · Traditional Capintec, Inc.03/30/1995SE
K920559Abbott Vertex AnalyzerJJJ · Traditional Abbott Laboratories03/19/1992SE
K900087Genesys 6000 Gamma CounterJJJ · Traditional Laboratory Technologies, Inc.07/19/1990SE
K896202MATRIX(TM)-96JJJ · Traditional Canberra Industries, Inc.01/02/1990SE
K894902SourcererJJJ · Traditional Oakfield Instruments, Ltd.10/17/1989SE
K884091SourcererJJJ · Traditional John Caunt Scientific , Ltd.02/02/1989SE
K884269Sample Identification Station Model 38010JJJ · Traditional Icn Micromedic Systems01/09/1989SE
K8740941205 Betaplate Liquid Scintillation CounterJJJ · Traditional Lkb Instruments, Inc.11/04/1987SE
K872430Iso-Data 500 Series Gamma CounterJJJ · Traditional Iso-Data, Inc.08/21/1987SE

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K782110Ria Kit, Rianen CortisolCGR · Traditional 01/26/1979SE
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K781495Rianen Assay System, 125I KitDNL · Traditional 09/14/1978SE

Questions and answers

When was Atomlight (Liquid Scintillation Solution cleared by the FDA?

Atomlight (Liquid Scintillation Solution (K801245) received a 510(k) decision of Substantially Equivalent on June 20, 1980, 24 days after the submission was received.

What is the product code of K801245?

The FDA product code is JJJ – Counter (Beta, Gamma) For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2320.