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FDA 510(k)

FilteredFlo Warming Blankets

K-Number: K232638 · 2023-10-24

Decision Date2023-10-24
Product CodeDWJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FilteredFlo Warming Blankets is the device name listed in this FDA 510(k) record. The listed applicant is Iob Medical, Inc.. It received FDA 510(k) clearance on 2023-10-24 under 510(k) number K232638. The device is classified under product code DWJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FilteredFlo Warming Blankets?

FilteredFlo Warming Blankets is a medical device that received FDA 510(k) clearance on 2023-10-24. The listed applicant is Iob Medical, Inc.. The 510(k) number is K232638.

When did FilteredFlo Warming Blankets receive FDA 510(k) clearance?

FilteredFlo Warming Blankets received FDA 510(k) clearance on 2023-10-24, under 510(k) number K232638.

Who is the listed applicant for FilteredFlo Warming Blankets?

The FDA 510(k) record lists Iob Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FilteredFlo Warming Blankets?

The FDA product code for FilteredFlo Warming Blankets is DWJ.

Other records listing Iob Medical, Inc. 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: DWJ)

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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