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FDA 510(k)

SIGMA PERIODIC ACID-SCHIFF STAIN 395

K-Number: K843752 · 1984-10-30

Decision Date1984-10-30
Product CodeHZT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SIGMA PERIODIC ACID-SCHIFF STAIN 395 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 1984-10-30 under 510(k) number K843752. The device is classified under product code HZT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGMA PERIODIC ACID-SCHIFF STAIN 395?

SIGMA PERIODIC ACID-SCHIFF STAIN 395 is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Sigma Chemical Co.. The 510(k) number is K843752.

When did SIGMA PERIODIC ACID-SCHIFF STAIN 395 receive FDA 510(k) clearance?

SIGMA PERIODIC ACID-SCHIFF STAIN 395 received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843752.

Who is the listed applicant for SIGMA PERIODIC ACID-SCHIFF STAIN 395?

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 PERIODIC ACID-SCHIFF STAIN 395?

The FDA product code for SIGMA PERIODIC ACID-SCHIFF STAIN 395 is HZT.

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.

View all 231 devices →

Related Devices (Code: HZT)

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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