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FDA 510(k)

CENTURION PRESSURE INJECTABLE EXTENSION SET

K-Number: K103562 · 2011-06-23

Decision Date2011-06-23
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTURION PRESSURE INJECTABLE EXTENSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Centurion Medical Products Corporation. It received FDA 510(k) clearance on 2011-06-23 under 510(k) number K103562. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTURION PRESSURE INJECTABLE EXTENSION SET?

CENTURION PRESSURE INJECTABLE EXTENSION SET is a medical device that received FDA 510(k) clearance on 2011-06-23. The listed applicant is Centurion Medical Products Corporation. The 510(k) number is K103562.

When did CENTURION PRESSURE INJECTABLE EXTENSION SET receive FDA 510(k) clearance?

CENTURION PRESSURE INJECTABLE EXTENSION SET received FDA 510(k) clearance on 2011-06-23, under 510(k) number K103562.

Who is the listed applicant for CENTURION PRESSURE INJECTABLE EXTENSION SET?

The FDA 510(k) record lists Centurion Medical Products Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTURION PRESSURE INJECTABLE EXTENSION SET?

The FDA product code for CENTURION PRESSURE INJECTABLE EXTENSION SET is FPA.

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 Centurion Medical Products Corporation 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.

Related Devices (Code: FPA)

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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