FDA 510(k)

DIAGNOSTICS PO 2 ELECTROLYTE

K-Number: K831013 · 1983-06-08

Decision Date1983-06-08

Product CodeCHL

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DIAGNOSTICS PO 2 ELECTROLYTE is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831013. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTICS PO 2 ELECTROLYTE?

DIAGNOSTICS PO 2 ELECTROLYTE is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K831013.

When did DIAGNOSTICS PO 2 ELECTROLYTE receive FDA 510(k) clearance?

DIAGNOSTICS PO 2 ELECTROLYTE received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831013.

Who is the listed applicant for DIAGNOSTICS PO 2 ELECTROLYTE?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIAGNOSTICS PO 2 ELECTROLYTE?

The FDA product code for DIAGNOSTICS PO 2 ELECTROLYTE is CHL.

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Other records listing Fisher Scientific Co., LLC as applicant

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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.