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FDA 510(k)

LYSING & HEMOGLOBIN S-REAGENT J & S

K-Number: K833444 · 1983-11-03

Decision Date1983-11-03
Product CodeGGK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LYSING & HEMOGLOBIN S-REAGENT J & S is the device name listed in this FDA 510(k) record. The listed applicant is Jasins & Sayles Associates, Inc.. It received FDA 510(k) clearance on 1983-11-03 under 510(k) number K833444. The device is classified under product code GGK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYSING & HEMOGLOBIN S-REAGENT J & S?

LYSING & HEMOGLOBIN S-REAGENT J & S is a medical device that received FDA 510(k) clearance on 1983-11-03. The listed applicant is Jasins & Sayles Associates, Inc.. The 510(k) number is K833444.

When did LYSING & HEMOGLOBIN S-REAGENT J & S receive FDA 510(k) clearance?

LYSING & HEMOGLOBIN S-REAGENT J & S received FDA 510(k) clearance on 1983-11-03, under 510(k) number K833444.

Who is the listed applicant for LYSING & HEMOGLOBIN S-REAGENT J & S?

The FDA 510(k) record lists Jasins & Sayles Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYSING & HEMOGLOBIN S-REAGENT J & S?

The FDA product code for LYSING & HEMOGLOBIN S-REAGENT J & S is GGK.

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 Jasins & Sayles Associates, Inc. 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.

Related Devices (Code: GGK)

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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