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FDA 510(k)

TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX

K-Number: K012771 · 2001-11-14

ApplicantPajunk GmbH
Decision Date2001-11-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX is the device name listed in this FDA 510(k) record. The listed applicant is Pajunk GmbH. It received FDA 510(k) clearance on 2001-11-14 under 510(k) number K012771. 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 TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX?

TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX is a medical device that received FDA 510(k) clearance on 2001-11-14. The listed applicant is Pajunk GmbH. The 510(k) number is K012771.

When did TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX receive FDA 510(k) clearance?

TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX received FDA 510(k) clearance on 2001-11-14, under 510(k) number K012771.

Who is the listed applicant for TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX?

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 TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX?

The FDA product code for TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX is GCJ.

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 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.

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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.

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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