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FDA 510(k)

STA AUTOMATED MULTI-PARAMETRIC ANALYZER

K-Number: K942117 · 1995-02-01

ApplicantAmerican Bioproducts Co.
Decision Date1995-02-01
Product CodeGKP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STA AUTOMATED MULTI-PARAMETRIC ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1995-02-01 under 510(k) number K942117. The device is classified under product code GKP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STA AUTOMATED MULTI-PARAMETRIC ANALYZER?

STA AUTOMATED MULTI-PARAMETRIC ANALYZER is a medical device that received FDA 510(k) clearance on 1995-02-01. The listed applicant is American Bioproducts Co.. The 510(k) number is K942117.

When did STA AUTOMATED MULTI-PARAMETRIC ANALYZER receive FDA 510(k) clearance?

STA AUTOMATED MULTI-PARAMETRIC ANALYZER received FDA 510(k) clearance on 1995-02-01, under 510(k) number K942117.

Who is the listed applicant for STA AUTOMATED MULTI-PARAMETRIC ANALYZER?

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

What is the FDA product code for STA AUTOMATED MULTI-PARAMETRIC ANALYZER?

The FDA product code for STA AUTOMATED MULTI-PARAMETRIC ANALYZER is GKP.

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Other records listing American Bioproducts 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.

K983460STAR AUTOMATED MULTI-PARAMETRIC ANALYZERK971519ASSERACHROM TPA TEST KITK964716STA LIATEST CONTROL [N]+[P] KITK964728STA-LIATEST D-DI TEST KITK964718STA D-DI CALIBRATOR KITK962675STA - LIATEST VWF TEST KIT

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Related Devices (Code: GKP)

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.

K242127ACL TOP Family 50 Series (ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS; ACL TOP 550 CTS; ACL TOP 350 CTS)Instrumentation Laboratory (IL) Co.K231031ACL TOP Family 70 SeriesInstrumentation Laboratory CompanyK160276ACL TOP (ACL TOP 700, ACL TOP 700 CTS, ACL TOP 700 LAS, ACL TOP 500 CTS, ACL TOP 300 CTS)Instrumentation Laboratory COK091980ACL TOP 700 LASInstrumentation Laboratory COK073377ACL TOP (WITH SYSTEM SOFTWARE V3.0.0)Instrumentation Laboratory COK063679ACL TOPInstrumentation Laboratory 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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