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FDA 510(k)

BLOOD-SMEARING INSTRUMENT (MINIPREP TM)

K-Number: K760007 · 1976-09-03

ApplicantGeometric Data, Div. Smithkline Corp.
Decision Date1976-09-03
Product CodeGKJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BLOOD-SMEARING INSTRUMENT (MINIPREP TM) 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 1976-09-03 under 510(k) number K760007. The device is classified under product code GKJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD-SMEARING INSTRUMENT (MINIPREP TM)?

BLOOD-SMEARING INSTRUMENT (MINIPREP TM) is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Geometric Data, Div. Smithkline Corp.. The 510(k) number is K760007.

When did BLOOD-SMEARING INSTRUMENT (MINIPREP TM) receive FDA 510(k) clearance?

BLOOD-SMEARING INSTRUMENT (MINIPREP TM) received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760007.

Who is the listed applicant for BLOOD-SMEARING INSTRUMENT (MINIPREP TM)?

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 BLOOD-SMEARING INSTRUMENT (MINIPREP TM)?

The FDA product code for BLOOD-SMEARING INSTRUMENT (MINIPREP TM) is GKJ.

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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: GKJ)

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.

K854962MICRO-MAT SYSTEMUlster Scientific, Inc.K854121MICRO-MAT SYSTEMPrevo Micro-Mat SystemK831558E-Z PREPCoulter Electronics, Inc.K811534HEMASPINNERGeometric Data, Div. Smithkline Corp.K771898AUTOMATED SLIDE SPINNERDynatech Cryomedical Co.

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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