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FDA 510(k)

PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE

K-Number: K854057 · 1985-12-05

ApplicantBeckman Instruments, Inc.
Decision Date1985-12-05
Product CodeJHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1985-12-05 under 510(k) number K854057. The device is classified under product code JHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE?

PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE is a medical device that received FDA 510(k) clearance on 1985-12-05. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K854057.

When did PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE receive FDA 510(k) clearance?

PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE received FDA 510(k) clearance on 1985-12-05, under 510(k) number K854057.

Who is the listed applicant for PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE?

The FDA product code for PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE is JHO.

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Related Devices (Code: JHO)

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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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