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FDA 510(k)

MICRO-MAT SYSTEM

K-Number: K854962 · 1985-12-23

ApplicantUlster Scientific, Inc.
Decision Date1985-12-23
Product CodeGKJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MICRO-MAT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ulster Scientific, Inc.. It received FDA 510(k) clearance on 1985-12-23 under 510(k) number K854962. 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 MICRO-MAT SYSTEM?

MICRO-MAT SYSTEM is a medical device that received FDA 510(k) clearance on 1985-12-23. The listed applicant is Ulster Scientific, Inc.. The 510(k) number is K854962.

When did MICRO-MAT SYSTEM receive FDA 510(k) clearance?

MICRO-MAT SYSTEM received FDA 510(k) clearance on 1985-12-23, under 510(k) number K854962.

Who is the listed applicant for MICRO-MAT SYSTEM?

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

What is the FDA product code for MICRO-MAT SYSTEM?

The FDA product code for MICRO-MAT SYSTEM is GKJ.

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Other records listing Ulster Scientific, Inc. 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.

K942620FEATHER-TOUCH SINGLE-STICK DEVICEK920562UNISTIKK902592EPC ELECTRONIC PIPETTING SYSTEMK895890AUTOPENK894474THE AUTOLET LITEK885340AIR DISPLACEMENT PIPETTE

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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.

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