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FDA 510(k)

ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18

K-Number: K851154 · 1985-05-13

ApplicantAstral Medical Systems
Decision Date1985-05-13
Product CodeJQT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 is the device name listed in this FDA 510(k) record. The listed applicant is Astral Medical Systems. It received FDA 510(k) clearance on 1985-05-13 under 510(k) number K851154. The device is classified under product code JQT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18?

ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is Astral Medical Systems. The 510(k) number is K851154.

When did ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 receive FDA 510(k) clearance?

ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 received FDA 510(k) clearance on 1985-05-13, under 510(k) number K851154.

Who is the listed applicant for ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18?

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

What is the FDA product code for ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18?

The FDA product code for ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 is JQT.

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 Astral Medical Systems 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.

K900506MODIFIED COATRON II AND COATRON JR.K851153COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGEK853734APOLLO DENSITOMETER

Related Devices (Code: JQT)

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.

K111356ASIMANAGER - ATArlington Scientific, Inc.K944185ISOSCANIsolab, Inc.K915332MODEL 795 FLUOROMETER/DENSITOMETERCiba Corning Diagnostics Corp.K885254TARGET READERV-Tech, Inc.K860645ELECTROPHORESIS DATA CENTER (EDC)Helena LaboratoriesK862956ICON READERHybritech, 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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