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FDA 510(k)

ABNORMAL PROTEIN ELECTROPHORESIS CONTROL

K-Number: K791031 · 1979-07-17

ApplicantBeckman Instruments, Inc.
Decision Date1979-07-17
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ABNORMAL PROTEIN ELECTROPHORESIS CONTROL 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 1979-07-17 under 510(k) number K791031. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABNORMAL PROTEIN ELECTROPHORESIS CONTROL?

ABNORMAL PROTEIN ELECTROPHORESIS CONTROL is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K791031.

When did ABNORMAL PROTEIN ELECTROPHORESIS CONTROL receive FDA 510(k) clearance?

ABNORMAL PROTEIN ELECTROPHORESIS CONTROL received FDA 510(k) clearance on 1979-07-17, under 510(k) number K791031.

Who is the listed applicant for ABNORMAL PROTEIN ELECTROPHORESIS CONTROL?

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 ABNORMAL PROTEIN ELECTROPHORESIS CONTROL?

The FDA product code for ABNORMAL PROTEIN ELECTROPHORESIS CONTROL is JJX.

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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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