Cleared Special

K112311 - ALP 501 RB PUMP SYSTEM

K112311 is an FDA 510(k) clearance for ALP 501 RB PUMP SYSTEM, manufactured by Currie Medical Specialties, Inc.. The device is a Class 2 Cardiovascular device with product code JOW cleared through the Special 510(k) pathway after a 21-day FDA review.

K112311 · Currie Medical Specialties, Inc. · Cardiovascular device
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Sep 2011
Decision
21d
Days
Class 2
Risk

K112311 is an FDA 510(k) clearance for the ALP 501 RB PUMP SYSTEM. Classified as Sleeve, Limb, Compressible (product code JOW), Class II - Special Controls.

Submitted by Currie Medical Specialties, Inc. (Monrovia, US). The FDA issued a Cleared decision on September 1, 2011 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5800 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Currie Medical Specialties, Inc. devices

FDA 510(k) Submission Details - K112311

510(k) Number K112311 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 11, 2011
Decision Date September 01, 2011
Days to Decision 21 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
104d faster than avg
Panel avg: 125d · This submission: 21d
Pathway characteristics
Modification to existing cleared device.

JOW Device Classification - Class 2, Special Controls

Product Code JOW Sleeve, Limb, Compressible
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5800
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 - JOW Sleeve, Limb, Compressible

All 247
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