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FDA 510(k)

STIMULONG PLUS CATHETER SET MODEL, VARIOUS

K-Number: K033018 · 2004-05-05

ApplicantPajunk GmbH
Decision Date2004-05-05
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STIMULONG PLUS CATHETER SET MODEL, VARIOUS is the device name listed in this FDA 510(k) record. The listed applicant is Pajunk GmbH. It received FDA 510(k) clearance on 2004-05-05 under 510(k) number K033018. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULONG PLUS CATHETER SET MODEL, VARIOUS?

STIMULONG PLUS CATHETER SET MODEL, VARIOUS is a medical device that received FDA 510(k) clearance on 2004-05-05. The listed applicant is Pajunk GmbH. The 510(k) number is K033018.

When did STIMULONG PLUS CATHETER SET MODEL, VARIOUS receive FDA 510(k) clearance?

STIMULONG PLUS CATHETER SET MODEL, VARIOUS received FDA 510(k) clearance on 2004-05-05, under 510(k) number K033018.

Who is the listed applicant for STIMULONG PLUS CATHETER SET MODEL, VARIOUS?

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

What is the FDA product code for STIMULONG PLUS CATHETER SET MODEL, VARIOUS?

The FDA product code for STIMULONG PLUS CATHETER SET MODEL, VARIOUS is CAZ.

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Other records listing Pajunk 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.

K113207SONO TAP, TUOHY SONOK113209CHIBA SONOK060563EPISPIN, EPISPIN II SAFETY, EPISPIN II, EPISPIN I, EPISPIN IVK053283UNIPLEX NANOLINE CANNULA, PLEXOLONG NANOLINE SET, STIMULONG NANOLINE SETK053282ADAPTABLE MONOPOLAR ELECTRODES WITH CERAMIC TIPK043130MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS

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Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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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