LX 300 Tissue Processor

FDA 510(k) K853938 · Innovative Medical Systems, Inc.

Substantially Equivalent

510(k) numberK853938

Submission

Device name
LX 300 Tissue Processor
Applicant
Innovative Medical Systems, Inc.
Ivyland, PA, US
Received
September 24, 1985
Decision date
October 10, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IEO – Processor, Tissue, Automated
Device class
Class I (low risk)
Regulation
21 CFR 864.3875
Specialty
Pathology

Other 510(k)s with product code IEO

510(k)DeviceApplicantDecision
K924590Microwave Automated Tissue ProcessorIEO · Traditional Innovative Medical Systems, Inc.12/29/1992SE
K883599LX-80 Automated Tissue Processor (Plastic)IEO · Traditional Innovative Medical Systems, Inc.09/02/1988SE
K881165Sakura HEM-480 Electron Microscopy ProcessorIEO · Traditional Sakura Finetek U.S.A., Inc.07/01/1988SE
K851054LX120 Tissue ProcessorIEO · Traditional Innovative Medical Systems, Inc.05/15/1985SE
K843506LKB 2189 UltroprocessorIEO · Traditional Lkb Instruments, Inc.11/30/1984SE
K834599Autotechnicon V Tissue Process SysIEO · Traditional Technicon Instruments Corp.02/04/1984SE
K831313Tissue-Tek V.I.P. 100/200IEO · Traditional Miles Laboratories, Inc.07/28/1983SE
K801513Tissue Processing SystemIEO · Traditional Innovative Medical Systems, Inc.07/28/1980SE
K801427Tissue-Tek III Mini-Rapid ProcessorIEO · Traditional Miles Laboratories, Inc.07/28/1980SE
K771308Tissue-Tek III V.I.P.IEO · Traditional Miles Laboratories, Inc.08/22/1977SE

More from Miles Laboratories, Inc.

510(k)DeviceDecision
K973035Viola II Dental Camera SystemEIA · Traditional 09/24/1997SE
K951469Bazooka SystemFNM · Traditional 06/28/1995SE
K933184Positive Airway Pressure SystemBZD · Traditional 11/28/1994SE
K924590Microwave Automated Tissue ProcessorIEO · Traditional 12/29/1992SE
K922081Labotech Automated Microtiter AnalyzerJJQ · Traditional 09/02/1992SE
K921005AutoloaderJQW · Traditional 04/29/1992SE
K915457Phaco 20/20 System IHQC · Traditional 02/24/1992SE
K915456Phaco 3000 LinearHQC · Traditional 02/12/1992SE
K883599LX-80 Automated Tissue Processor (Plastic)IEO · Traditional 09/02/1988SE
K880745LX-100 Slide StainerKPA · Traditional 04/27/1988SE

Questions and answers

When was LX 300 Tissue Processor cleared by the FDA?

LX 300 Tissue Processor (K853938) received a 510(k) decision of Substantially Equivalent on October 10, 1985, 16 days after the submission was received.

What is the product code of K853938?

The FDA product code is IEO – Processor, Tissue, Automated, a Class I (low risk) device regulated under 21 CFR 864.3875.