FDA 510(k)

BARBITAL BUFFER

K-Number: K771721 · 1977-10-18

Decision Date1977-10-18

Product Code

DecisionSubstantially Equivalent

Device Summary

BARBITAL BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1977-10-18 under 510(k) number K771721. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARBITAL BUFFER?

BARBITAL BUFFER is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is Sigma Chemical Co.. The 510(k) number is K771721.

When did BARBITAL BUFFER receive FDA 510(k) clearance?

BARBITAL BUFFER received FDA 510(k) clearance on 1977-10-18, under 510(k) number K771721.

Who is the listed applicant for BARBITAL BUFFER?

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

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Other records listing Sigma Chemical Co. as applicant

K933694SIGMA GLUCOSE REAGENT K933678SIGMA CALCIUM REAGENT K933696SIGMA ELECTROLYTE REFERENCE REAGENT K933691SIGMA CO2 ALKALINE BUFFER REAGENT K933679SIGMA BUN REAGENT K933703SIGMA WASH CONCENTRATE SOLUTION

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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.