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FDA 510(k)

HEMASTAIN WRIGHT STAIN

K-Number: K760486 · 1976-08-30

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1976-08-30
Product Code
DecisionSubstantially Equivalent

Device Summary

HEMASTAIN WRIGHT STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Geometric Data, Div. Smithkline Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760486. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMASTAIN WRIGHT STAIN?

HEMASTAIN WRIGHT STAIN is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K760486.

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

HEMASTAIN WRIGHT STAIN received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760486.

Who is the listed applicant for HEMASTAIN WRIGHT STAIN?

The FDA 510(k) record lists Geometric Data, Div. Smithkline Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Geometric Data, Div. Smithkline Corp. 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.

K841852AUTOLYZER 800K811534HEMASPINNERK791041HEMATRAK ABNORMAL RECOGNITIONK790816HEMATRAK MODEL 480K791108CONTEXT FILTERK790042STAIN, HEMASTAIN RETIC

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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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