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FDA 510(k)

SOMAS CHLORIDE ASSAY KIT

K-Number: K833787 · 1984-01-11

ApplicantSomas Medical Industries, Inc.
Decision Date1984-01-11
Product Code
DecisionSubstantially Equivalent

Device Summary

SOMAS CHLORIDE ASSAY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Somas Medical Industries, Inc.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K833787. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOMAS CHLORIDE ASSAY KIT?

SOMAS CHLORIDE ASSAY KIT is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Somas Medical Industries, Inc.. The 510(k) number is K833787.

When did SOMAS CHLORIDE ASSAY KIT receive FDA 510(k) clearance?

SOMAS CHLORIDE ASSAY KIT received FDA 510(k) clearance on 1984-01-11, under 510(k) number K833787.

Who is the listed applicant for SOMAS CHLORIDE ASSAY KIT?

The FDA 510(k) record lists Somas Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Somas Medical Industries, 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.

K862179SOMAS LIQUID URINE CONTROLK842134SOMAS COOMASIE BLUE TOTAL PROTEIN ASSAYK840486TOTAL BILIRUBIN REAGENTK840974SOMAS HUMAN SPINAL FLUID CONTROLK840485TOTAL IRON UIBC/TIBC ASSAY

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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