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FDA 510(k)

VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596

K-Number: K020752 · 2002-05-02

Decision Date2002-05-02
Product CodeMID
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deutschland GmbH. It received FDA 510(k) clearance on 2002-05-02 under 510(k) number K020752. The device is classified under product code MID. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596?

VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596 is a medical device that received FDA 510(k) clearance on 2002-05-02. The listed applicant is Pharmacia Deutschland GmbH. The 510(k) number is K020752.

When did VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596 receive FDA 510(k) clearance?

VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596 received FDA 510(k) clearance on 2002-05-02, under 510(k) number K020752.

Who is the listed applicant for VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596?

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

What is the FDA product code for VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596?

The FDA product code for VARELISA CARDIOLIPIN IGG ANTIBODIES, MODELS 15548 & 15596 is MID.

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 Pharmacia Deutschland GmbH 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: MID)

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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