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FDA 510(k)

PAJUNK MODULAR HANDLE INSTRUMENTS

K-Number: K033249 · 2004-03-05

ApplicantPajunk GmbH
Decision Date2004-03-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PAJUNK MODULAR HANDLE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Pajunk GmbH. It received FDA 510(k) clearance on 2004-03-05 under 510(k) number K033249. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAJUNK MODULAR HANDLE INSTRUMENTS?

PAJUNK MODULAR HANDLE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2004-03-05. The listed applicant is Pajunk GmbH. The 510(k) number is K033249.

When did PAJUNK MODULAR HANDLE INSTRUMENTS receive FDA 510(k) clearance?

PAJUNK MODULAR HANDLE INSTRUMENTS received FDA 510(k) clearance on 2004-03-05, under 510(k) number K033249.

Who is the listed applicant for PAJUNK MODULAR HANDLE INSTRUMENTS?

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 PAJUNK MODULAR HANDLE INSTRUMENTS?

The FDA product code for PAJUNK MODULAR HANDLE INSTRUMENTS is GCJ.

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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: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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