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FDA 510(k)

DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML

K-Number: K020666 · 2002-06-24

Decision Date2002-06-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 2002-06-24 under 510(k) number K020666. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML?

DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML is a medical device that received FDA 510(k) clearance on 2002-06-24. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K020666.

When did DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML receive FDA 510(k) clearance?

DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML received FDA 510(k) clearance on 2002-06-24, under 510(k) number K020666.

Who is the listed applicant for DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML?

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

What is the FDA product code for DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML?

The FDA product code for DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML is FMF.

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.

Other records listing Baxter Healthcare 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.

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Related Devices (Code: FMF)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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