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FDA 510(k)

MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI

K-Number: K915896 · 1992-05-04

ApplicantDynatech Laboratories, Inc.
Decision Date1992-05-04
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI 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 1992-05-04 under 510(k) number K915896. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI?

MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI is a medical device that received FDA 510(k) clearance on 1992-05-04. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K915896.

When did MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI receive FDA 510(k) clearance?

MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI received FDA 510(k) clearance on 1992-05-04, under 510(k) number K915896.

Who is the listed applicant for MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI?

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 ML2250/MODI?

The FDA product code for MICROLITE MICROTITER PLATE LUMINOMETER ML2250/MODI is JJQ.

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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.

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Related Devices (Code: JJQ)

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, 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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