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FDA 510(k)

CARBON DIOXIDE CUP REAGENT & REF.RGT.

K-Number: K800218 · 1980-02-26

ApplicantFisher Scientific Co., LLC
Decision Date1980-02-26
Product CodeJFL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARBON DIOXIDE CUP REAGENT & REF.RGT. 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 1980-02-26 under 510(k) number K800218. The device is classified under product code JFL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBON DIOXIDE CUP REAGENT & REF.RGT.?

CARBON DIOXIDE CUP REAGENT & REF.RGT. is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K800218.

When did CARBON DIOXIDE CUP REAGENT & REF.RGT. receive FDA 510(k) clearance?

CARBON DIOXIDE CUP REAGENT & REF.RGT. received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800218.

Who is the listed applicant for CARBON DIOXIDE CUP REAGENT & REF.RGT.?

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 CARBON DIOXIDE CUP REAGENT & REF.RGT.?

The FDA product code for CARBON DIOXIDE CUP REAGENT & REF.RGT. is JFL.

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Other records listing Fisher Scientific Co., LLC 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.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: JFL)

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

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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