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FDA 510(k)

REAGENT KIT, CHLORIDE/CARBON DIOXIDE

K-Number: K790045 · 1979-02-22

Decision Date1979-02-22
Product CodeJFS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REAGENT KIT, CHLORIDE/CARBON DIOXIDE is the device name listed in this FDA 510(k) record. The listed applicant is J.T. Baker Chemical Co.. It received FDA 510(k) clearance on 1979-02-22 under 510(k) number K790045. The device is classified under product code JFS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT KIT, CHLORIDE/CARBON DIOXIDE?

REAGENT KIT, CHLORIDE/CARBON DIOXIDE is a medical device that received FDA 510(k) clearance on 1979-02-22. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K790045.

When did REAGENT KIT, CHLORIDE/CARBON DIOXIDE receive FDA 510(k) clearance?

REAGENT KIT, CHLORIDE/CARBON DIOXIDE received FDA 510(k) clearance on 1979-02-22, under 510(k) number K790045.

Who is the listed applicant for REAGENT KIT, CHLORIDE/CARBON DIOXIDE?

The FDA 510(k) record lists J.T. Baker Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REAGENT KIT, CHLORIDE/CARBON DIOXIDE?

The FDA product code for REAGENT KIT, CHLORIDE/CARBON DIOXIDE is JFS.

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 J.T. Baker Chemical Co. 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.

View all 54 devices →

Related Devices (Code: JFS)

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.

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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