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FDA 510(k)

BECKMAN ELECTROPHORESIS OVEN/INCUBATOR

K-Number: K791077 · 1979-07-24

Decision Date1979-07-24
Product CodeJRJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN ELECTROPHORESIS OVEN/INCUBATOR 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 1979-07-24 under 510(k) number K791077. The device is classified under product code JRJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN ELECTROPHORESIS OVEN/INCUBATOR?

BECKMAN ELECTROPHORESIS OVEN/INCUBATOR is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K791077.

When did BECKMAN ELECTROPHORESIS OVEN/INCUBATOR receive FDA 510(k) clearance?

BECKMAN ELECTROPHORESIS OVEN/INCUBATOR received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791077.

Who is the listed applicant for BECKMAN ELECTROPHORESIS OVEN/INCUBATOR?

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 BECKMAN ELECTROPHORESIS OVEN/INCUBATOR?

The FDA product code for BECKMAN ELECTROPHORESIS OVEN/INCUBATOR is JRJ.

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.

Other records listing Beckman Instruments, 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.

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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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