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FDA 510(k)

LKB 2189 ULTROPROCESSOR

K-Number: K843506 · 1984-11-30

ApplicantLkb Instruments, Inc.
Decision Date1984-11-30
Product CodeIEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LKB 2189 ULTROPROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1984-11-30 under 510(k) number K843506. The device is classified under product code IEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LKB 2189 ULTROPROCESSOR?

LKB 2189 ULTROPROCESSOR is a medical device that received FDA 510(k) clearance on 1984-11-30. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K843506.

When did LKB 2189 ULTROPROCESSOR receive FDA 510(k) clearance?

LKB 2189 ULTROPROCESSOR received FDA 510(k) clearance on 1984-11-30, under 510(k) number K843506.

Who is the listed applicant for LKB 2189 ULTROPROCESSOR?

The FDA 510(k) record lists Lkb Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LKB 2189 ULTROPROCESSOR?

The FDA product code for LKB 2189 ULTROPROCESSOR is IEO.

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Related Devices (Code: IEO)

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K924590MICROWAVE AUTOMATED TISSUE PROCESSORInnovative Medical Systems, Inc.K883599LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)Innovative Medical Systems, Inc.K881165SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSORSakura Finetek U.S.A., Inc.K853938LX 300 TISSUE PROCESSORInnovative Medical Systems, Inc.K851054LX120 TISSUE PROCESSORInnovative Medical Systems, Inc.K834599AUTOTECHNICON V TISSUE PROCESS SYSTechnicon Instruments Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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