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FDA 510(k)

BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM

K-Number: K801896 · 1980-09-16

ApplicantBeckman Instruments, Inc.
Decision Date1980-09-16
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM 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 1980-09-16 under 510(k) number K801896. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM?

BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K801896.

When did BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM receive FDA 510(k) clearance?

BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801896.

Who is the listed applicant for BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM?

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 ELECTROLYTE-2 SODIUM/POTASSIUM?

The FDA product code for BECKMAN ELECTROLYTE-2 SODIUM/POTASSIUM is JGS.

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Other records listing Beckman Instruments, Inc. as applicant

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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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