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FDA 510(k)

WRIGHT RAPID STAIN

K-Number: K781384 · 1978-08-21

Decision Date1978-08-21
Product CodeIAF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

WRIGHT RAPID STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Mfg Chemists, Inc.. It received FDA 510(k) clearance on 1978-08-21 under 510(k) number K781384. The device is classified under product code IAF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT RAPID STAIN?

WRIGHT RAPID STAIN is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Mfg Chemists, Inc.. The 510(k) number is K781384.

When did WRIGHT RAPID STAIN receive FDA 510(k) clearance?

WRIGHT RAPID STAIN received FDA 510(k) clearance on 1978-08-21, under 510(k) number K781384.

Who is the listed applicant for WRIGHT RAPID STAIN?

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

What is the FDA product code for WRIGHT RAPID STAIN?

The FDA product code for WRIGHT RAPID STAIN is IAF.

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.

Related Devices (Code: IAF)

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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