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FDA 510(k)

PDA SYSTEM

K-Number: K842522 · 1984-08-02

ApplicantAbbott Laboratories
Decision Date1984-08-02
Product CodeJJG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PDA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K842522. The device is classified under product code JJG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDA SYSTEM?

PDA SYSTEM is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Abbott Laboratories. The 510(k) number is K842522.

When did PDA SYSTEM receive FDA 510(k) clearance?

PDA SYSTEM received FDA 510(k) clearance on 1984-08-02, under 510(k) number K842522.

Who is the listed applicant for PDA SYSTEM?

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

What is the FDA product code for PDA SYSTEM?

The FDA product code for PDA SYSTEM is JJG.

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Related Devices (Code: JJG)

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.

K972409AG CHEMISTRY ANALYZER SYSTEMLandmark Scientific, Inc.K942782PICCOLO(TM)Abaxis, Inc.K934592EPOC 2000 POINT-OF-CARE ANALYZER AND EPOC 5-CHEMISTRY REAGENT ROTORAbaxis, Inc.K920942OLYMPUS AU800 CLINICAL CHEMISTRY ANALYZEROlympus Corp.K910222COBAS ALPHARoche Diagnostic Systems, Inc.K903626BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISABeckman Instruments, Inc.

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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