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FDA 510(k)

POSID SAMPLER

K-Number: K860508 · 1986-05-02

ApplicantOrganon Teknika Corp.
Decision Date1986-05-02
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

POSID SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Organon Teknika Corp.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K860508. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSID SAMPLER?

POSID SAMPLER is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Organon Teknika Corp.. The 510(k) number is K860508.

When did POSID SAMPLER receive FDA 510(k) clearance?

POSID SAMPLER received FDA 510(k) clearance on 1986-05-02, under 510(k) number K860508.

Who is the listed applicant for POSID SAMPLER?

The FDA 510(k) record lists Organon Teknika Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POSID SAMPLER?

The FDA product code for POSID SAMPLER is JQW.

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Other records listing Organon Teknika 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.

K003104BACT/ALERT CSRK000492MDA D-DIMERK000378BACT/ALERT MB CULTURE BOTTLEK994343BACT/ALERT SVK993423BACT/ALERT SAK993421BACT/ALERT SN

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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