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FDA 510(k)

SIGMA PROCEDURE 47-UV

K-Number: K842013 · 1984-06-25

ApplicantSigma Chemical Co.
Decision Date1984-06-25
Product CodeCGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SIGMA PROCEDURE 47-UV 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 1984-06-25 under 510(k) number K842013. The device is classified under product code CGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGMA PROCEDURE 47-UV?

SIGMA PROCEDURE 47-UV is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Sigma Chemical Co.. The 510(k) number is K842013.

When did SIGMA PROCEDURE 47-UV receive FDA 510(k) clearance?

SIGMA PROCEDURE 47-UV received FDA 510(k) clearance on 1984-06-25, under 510(k) number K842013.

Who is the listed applicant for SIGMA PROCEDURE 47-UV?

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 PROCEDURE 47-UV?

The FDA product code for SIGMA PROCEDURE 47-UV is CGS.

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Other records listing Sigma Chemical Co. as applicant

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Related Devices (Code: CGS)

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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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