Cleared Traditional

K121108 - DOPPLEX ABILITY

K121108 is an FDA 510(k) clearance for DOPPLEX ABILITY, manufactured by Huntleigh Healthcare. The device is a Class 2 Cardiovascular device with product code JOM cleared through the Traditional 510(k) pathway after a 266-day FDA review.

K121108 · Huntleigh Healthcare · Cardiovascular device
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Jan 2013
Decision
266d
Days
Class 2
Risk

K121108 is an FDA 510(k) clearance for the DOPPLEX ABILITY. Classified as Plethysmograph, Photoelectric, Pneumatic Or Hydraulic (product code JOM), Class II - Special Controls.

Submitted by Huntleigh Healthcare (Cardiff, GB). The FDA issued a Cleared decision on January 3, 2013 after a review of 266 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2780 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Huntleigh Healthcare devices

FDA 510(k) Submission Details - K121108

510(k) Number K121108 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 12, 2012
Decision Date January 03, 2013
Days to Decision 266 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
141d slower than avg
Panel avg: 125d · This submission: 266d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JOM Device Classification - Class 2, Special Controls

Product Code JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2780
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

All 8
Devices cleared under the same product code (JOM) and FDA review panel - the closest regulatory comparables to K121108.
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