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FDA 510(k)

PARAGON SERUM PROTEIN ELECTROPHORESIS

K-Number: K802592 · 1980-11-12

ApplicantBeckman Instruments, Inc.
Decision Date1980-11-12
Product CodeCEF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARAGON SERUM PROTEIN ELECTROPHORESIS 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 1980-11-12 under 510(k) number K802592. The device is classified under product code CEF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAGON SERUM PROTEIN ELECTROPHORESIS?

PARAGON SERUM PROTEIN ELECTROPHORESIS is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K802592.

When did PARAGON SERUM PROTEIN ELECTROPHORESIS receive FDA 510(k) clearance?

PARAGON SERUM PROTEIN ELECTROPHORESIS received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802592.

Who is the listed applicant for PARAGON SERUM PROTEIN ELECTROPHORESIS?

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 SERUM PROTEIN ELECTROPHORESIS?

The FDA product code for PARAGON SERUM PROTEIN ELECTROPHORESIS is CEF.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: CEF)

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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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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