510(k) Report

FDA applicant

Innercool Therapies, Inc.- A Delaware Corporation

San Diego, CA1 decision2008–20081 recall

FDA records 1 decision for Innercool Therapies, Inc.- A Delaware Corporation (San Diego, CA) in 2008: 1 510(k) clearance. All are in product code NCX (System, Hypothermia, Intravenous, Cooling). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Innercool Therapies, Inc.- A Delaware Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

1in 2014

2014: 1
2008high 1 (2014) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Innercool Therapies, Inc.- A Delaware Corporation by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Innercool Therapies, Inc.- A Delaware…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • NCXSystem, Hypothermia, Intravenous, Cooling1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K080908Innercool Therapies, Inc., Rapidblue SystemInnercool Therapies, Inc.- A Delaware Corporation · 20081cites it

What has FDA decided for it lately?

  • K080908Innercool Therapies, Inc., Rapidblue SystemInnercool Therapies, Inc.- A Delaware Corporation · 20081 recall

The one decision as Innercool Therapies, Inc.- A Delaware Corporation →

What has been recalled?

1 recall linked to its devices; the latest:

  • K080908InnerCool RTx Endovascular System, Model Numbers: 861470 (120V), 861472 (240V). Product…Jan 13, 2014Class II

Other applicant names beginning “Innercool”

FDA records each applicant name separately; these may or may not be the same firm.

Innercool Therapies 2