FDA 510(k)

IRON STAIN PROCEDURE HT20

K-Number: K833388 · 1983-10-31

Decision Date1983-10-31

Product CodeLED

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

IRON STAIN PROCEDURE HT20 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 1983-10-31 under 510(k) number K833388. The device is classified under product code LED. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IRON STAIN PROCEDURE HT20?

IRON STAIN PROCEDURE HT20 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Sigma Chemical Co.. The 510(k) number is K833388.

When did IRON STAIN PROCEDURE HT20 receive FDA 510(k) clearance?

IRON STAIN PROCEDURE HT20 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K833388.

Who is the listed applicant for IRON STAIN PROCEDURE HT20?

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 IRON STAIN PROCEDURE HT20?

The FDA product code for IRON STAIN PROCEDURE HT20 is LED.

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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.