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FDA 510(k)

AUTOMATED SLIDE SPINNER

K-Number: K771898 · 1977-10-18

ApplicantDynatech Cryomedical Co.
Decision Date1977-10-18
Product CodeGKJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AUTOMATED SLIDE SPINNER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Cryomedical Co.. It received FDA 510(k) clearance on 1977-10-18 under 510(k) number K771898. 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 AUTOMATED SLIDE SPINNER?

AUTOMATED SLIDE SPINNER is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is Dynatech Cryomedical Co.. The 510(k) number is K771898.

When did AUTOMATED SLIDE SPINNER receive FDA 510(k) clearance?

AUTOMATED SLIDE SPINNER received FDA 510(k) clearance on 1977-10-18, under 510(k) number K771898.

Who is the listed applicant for AUTOMATED SLIDE SPINNER?

The FDA 510(k) record lists Dynatech Cryomedical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMATED SLIDE SPINNER?

The FDA product code for AUTOMATED SLIDE SPINNER is GKJ.

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.

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Other records listing Dynatech Cryomedical 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.

K771815SIGMOSCOPEK770896COLPOSCOPE MODEL IIK770614MONITOR, GAS MANIFOLDK761205DYNATECH JD7/JD7P COLPOSCOPEK760763COLPOSCOPE (DYNATECH COLPOSCOPE-MODEL I

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.K760007BLOOD-SMEARING INSTRUMENT (MINIPREP TM)Geometric Data, Div. Smithkline Corp.

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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