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FDA 510(k)

DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON

K-Number: K831012 · 1983-06-08

ApplicantFisher Scientific Co., LLC
Decision Date1983-06-08
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON 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 K831012. 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 PCO2 ELECTROLYTE W/CARBON?

DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON 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 K831012.

When did DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON receive FDA 510(k) clearance?

DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831012.

Who is the listed applicant for DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON?

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 PCO2 ELECTROLYTE W/CARBON?

The FDA product code for DIAGNOSTICS PCO2 ELECTROLYTE W/CARBON 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.

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