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FDA 510(k)

SIGMA REAGENT SYSTEM NO. 885

K-Number: K822733 · 1982-12-03

Decision Date1982-12-03
Product CodeJBE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SIGMA REAGENT SYSTEM NO. 885 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 1982-12-03 under 510(k) number K822733. The device is classified under product code JBE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGMA REAGENT SYSTEM NO. 885?

SIGMA REAGENT SYSTEM NO. 885 is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Sigma Chemical Co.. The 510(k) number is K822733.

When did SIGMA REAGENT SYSTEM NO. 885 receive FDA 510(k) clearance?

SIGMA REAGENT SYSTEM NO. 885 received FDA 510(k) clearance on 1982-12-03, under 510(k) number K822733.

Who is the listed applicant for SIGMA REAGENT SYSTEM NO. 885?

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

What is the FDA product code for SIGMA REAGENT SYSTEM NO. 885?

The FDA product code for SIGMA REAGENT SYSTEM NO. 885 is JBE.

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 Sigma 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.

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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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