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FDA 510(k)

ELECTRA AUTOMATIC SAMPLER

K-Number: K864875 · 1987-02-13

ApplicantMedical Laboratory Automation Systems, Inc.
Decision Date1987-02-13
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTRA AUTOMATIC SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Laboratory Automation Systems, Inc.. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K864875. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRA AUTOMATIC SAMPLER?

ELECTRA AUTOMATIC SAMPLER is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Medical Laboratory Automation Systems, Inc.. The 510(k) number is K864875.

When did ELECTRA AUTOMATIC SAMPLER receive FDA 510(k) clearance?

ELECTRA AUTOMATIC SAMPLER received FDA 510(k) clearance on 1987-02-13, under 510(k) number K864875.

Who is the listed applicant for ELECTRA AUTOMATIC SAMPLER?

The FDA 510(k) record lists Medical Laboratory Automation Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRA AUTOMATIC SAMPLER?

The FDA product code for ELECTRA AUTOMATIC SAMPLER is JQW.

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Other records listing Medical Laboratory Automation Systems, 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.

K962664ELECTRA 1800C AUTOMATIC COAGULATION ANALYZERK944227ELECTRA 1400C AUTOMATIC COAGULATION ANALYZERK931206ELECTRA 1600C AUTOMATIC COAGULATION TIMERK923220THROMBIN CLOT TIME TEST PROCEDUREK903638GASTRO-INTESTINAL ACCU-CULSHURE TMK903406VIRAL ACCU-CULSHURE TM

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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