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FDA 510(k)

EMAX PRECISION MICROPLATE READER

K-Number: K883302 · 1988-09-13

ApplicantMolecular Devices Corp.
Decision Date1988-09-13
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EMAX PRECISION MICROPLATE READER is the device name listed in this FDA 510(k) record. The listed applicant is Molecular Devices Corp.. It received FDA 510(k) clearance on 1988-09-13 under 510(k) number K883302. 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 EMAX PRECISION MICROPLATE READER?

EMAX PRECISION MICROPLATE READER is a medical device that received FDA 510(k) clearance on 1988-09-13. The listed applicant is Molecular Devices Corp.. The 510(k) number is K883302.

When did EMAX PRECISION MICROPLATE READER receive FDA 510(k) clearance?

EMAX PRECISION MICROPLATE READER received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883302.

Who is the listed applicant for EMAX PRECISION MICROPLATE READER?

The FDA 510(k) record lists Molecular Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMAX PRECISION MICROPLATE READER?

The FDA product code for EMAX PRECISION MICROPLATE READER is JJQ.

Related Clinical Trials

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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Other records listing Molecular Devices Corp. 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.

K892063THERMOMAX MICROPLATE READER, MODIFICATIONK881803UVMAX KINETIC MICROPLATE READERK863802VMAX KINETIC MICROPLATE READER

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

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

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