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FDA 510(k)

VMAX KINETIC MICROPLATE READER

K-Number: K863802 · 1986-11-05

ApplicantMolecular Devices Corp.
Decision Date1986-11-05
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VMAX KINETIC 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 1986-11-05 under 510(k) number K863802. 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 VMAX KINETIC MICROPLATE READER?

VMAX KINETIC MICROPLATE READER is a medical device that received FDA 510(k) clearance on 1986-11-05. The listed applicant is Molecular Devices Corp.. The 510(k) number is K863802.

When did VMAX KINETIC MICROPLATE READER receive FDA 510(k) clearance?

VMAX KINETIC MICROPLATE READER received FDA 510(k) clearance on 1986-11-05, under 510(k) number K863802.

Who is the listed applicant for VMAX KINETIC 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 VMAX KINETIC MICROPLATE READER?

The FDA product code for VMAX KINETIC 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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, MODIFICATIONK883302EMAX PRECISION MICROPLATE READERK881803UVMAX 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

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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