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FDA 510(k)

MICROLITE MICROTITER PLATE LUMINOMETER ML2200

K-Number: K920888 · 1992-03-19

ApplicantDynatech Laboratories, Inc.
Decision Date1992-03-19
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROLITE MICROTITER PLATE LUMINOMETER ML2200 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1992-03-19 under 510(k) number K920888. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROLITE MICROTITER PLATE LUMINOMETER ML2200?

MICROLITE MICROTITER PLATE LUMINOMETER ML2200 is a medical device that received FDA 510(k) clearance on 1992-03-19. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K920888.

When did MICROLITE MICROTITER PLATE LUMINOMETER ML2200 receive FDA 510(k) clearance?

MICROLITE MICROTITER PLATE LUMINOMETER ML2200 received FDA 510(k) clearance on 1992-03-19, under 510(k) number K920888.

Who is the listed applicant for MICROLITE MICROTITER PLATE LUMINOMETER ML2200?

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

What is the FDA product code for MICROLITE MICROTITER PLATE LUMINOMETER ML2200?

The FDA product code for MICROLITE MICROTITER PLATE LUMINOMETER ML2200 is KHO.

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Other records listing Dynatech Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962265MLX MICROTITER PLATE LUMINOMETERK934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)K943701MRX MICROPLATE READERK923456MICROLITE MICROTITER PLATE LUMINOMETER ML3000K915896MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODIK913590MICROLITE ML 1000 MICROTITER PLATE LUMINOMETER

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Related Devices (Code: KHO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112161AQT90 FLEX ANALYZER, AQT90 FLEX MYOGLOBIN TEST KIT, AQT90 FLEX LQC MULTI-CHECK, LVLS 1-3, AQT90 FLEX MYO CAL CARTRIDGE..Radiometer Medical ApsK973547TRIAGE STATMETERBiosite IncorporatedK971103AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEMTosoh Medics, Inc.K962919VITROS IMMUNODIAGNOSTIC SYSTEMJohnson & Johnson Clinical Diagnostics, Inc.K952719BIOCIRCUITS IOS (IN-OFFICE SYSTEM)Biocircuits Corp.K950415FLUOROSCAN NEONATALIsolab, Inc.

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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