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FDA 510(k)

REAGENT, AMP BUFFER DIAGNOSTIC

K-Number: K760397 · 1976-11-01

ApplicantJ.T. Baker Chemical Co.
Decision Date1976-11-01
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REAGENT, AMP BUFFER DIAGNOSTIC 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 1976-11-01 under 510(k) number K760397. The device is classified under product code CJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT, AMP BUFFER DIAGNOSTIC?

REAGENT, AMP BUFFER DIAGNOSTIC is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K760397.

When did REAGENT, AMP BUFFER DIAGNOSTIC receive FDA 510(k) clearance?

REAGENT, AMP BUFFER DIAGNOSTIC received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760397.

Who is the listed applicant for REAGENT, AMP BUFFER DIAGNOSTIC?

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, AMP BUFFER DIAGNOSTIC?

The FDA product code for REAGENT, AMP BUFFER DIAGNOSTIC is CJE.

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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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