Iso-Data 100 Series Gamma Counter

FDA 510(k) K872429 · Iso-Data, Inc.

Substantially Equivalent

510(k) numberK872429

Submission

Device name
Iso-Data 100 Series Gamma Counter
Applicant
Iso-Data, Inc.
Rolling Meadows, IL, US
Received
June 22, 1987
Decision date
August 21, 1987
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

510(k)DeviceApplicantDecision
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

More from Iso-Data, Inc.

510(k)DeviceDecision
K872430Iso-Data 500 Series Gamma CounterJJJ · Traditional 08/21/1987SE
K843434Iso-Data Centrifuges 1-A, 101, 2D, Etc.JQC · Traditional 10/05/1984SE
K843365Iso-Data Immunoassay Network SystemJQP · Traditional 09/27/1984SE
K810631DPM CalculatorJQP · Traditional 03/27/1981SE
K780813Idi GDR Data Reduction System · Traditional 06/28/1978SE
K780790Idi 200 Gamma CounterJJJ · Traditional 06/22/1978SE

Questions and answers

When was Iso-Data 100 Series Gamma Counter cleared by the FDA?

Iso-Data 100 Series Gamma Counter (K872429) received a 510(k) decision of Substantially Equivalent on August 21, 1987, 60 days after the submission was received.

What is the product code of K872429?

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