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FDA 510(k)

FOAM RING PORT PROTECTOR

K-Number: K062261 · 2007-04-09

Decision Date2007-04-09
Product CodeOBK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FOAM RING PORT PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Inspired Ideas, Incorporated. It received FDA 510(k) clearance on 2007-04-09 under 510(k) number K062261. The device is classified under product code OBK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOAM RING PORT PROTECTOR?

FOAM RING PORT PROTECTOR is a medical device that received FDA 510(k) clearance on 2007-04-09. The listed applicant is Inspired Ideas, Incorporated. The 510(k) number is K062261.

When did FOAM RING PORT PROTECTOR receive FDA 510(k) clearance?

FOAM RING PORT PROTECTOR received FDA 510(k) clearance on 2007-04-09, under 510(k) number K062261.

Who is the listed applicant for FOAM RING PORT PROTECTOR?

The FDA 510(k) record lists Inspired Ideas, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOAM RING PORT PROTECTOR?

The FDA product code for FOAM RING PORT PROTECTOR is OBK.

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.

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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