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FDA 510(k)

HEMASTAIN FIXATIVE

K-Number: K760485 · 1976-08-30

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1976-08-30
Product CodeKQC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HEMASTAIN FIXATIVE 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 K760485. The device is classified under product code KQC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMASTAIN FIXATIVE?

HEMASTAIN FIXATIVE 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 K760485.

When did HEMASTAIN FIXATIVE receive FDA 510(k) clearance?

HEMASTAIN FIXATIVE received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760485.

Who is the listed applicant for HEMASTAIN FIXATIVE?

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

What is the FDA product code for HEMASTAIN FIXATIVE?

The FDA product code for HEMASTAIN FIXATIVE is KQC.

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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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Related Devices (Code: KQC)

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.

K882873FIELDTEX HEMATOXYLINAnatech, Ltd.K852843GENERAL DIAGNOSTICS COAG-A-MATE XCWarner-Lambert Co.K843619RETIC-SETR&D Systems, Inc.K841848RETIC-SETR&D Systems, Inc.K792550PONCEAU S STAIN SETElectrophoresis Corp. of AmericaK792496VOLU-SOL NMB RETICULOCYTE STAINVolu Sol Medical Industries

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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