Cleared Traditional

K952671 - RATESAVER PLUS

K952671 is an FDA 510(k) clearance for RATESAVER PLUS, manufactured by Entracare Corp.. The device is a Class 2 General Hospital device with product code LZH cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K952671 · Entracare Corp. · General Hospital
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Aug 1995
Decision
67d
Days
Class 2
Risk

K952671 is an FDA 510(k) clearance for the RATESAVER PLUS. Classified as Pump, Infusion, Enteral (product code LZH), Class II - Special Controls.

Submitted by Entracare Corp. (Lenexa, US). The FDA issued a Cleared decision on August 18, 1995 after a review of 67 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Entracare Corp. devices

FDA 510(k) Submission Details - K952671

510(k) Number K952671 FDA.gov
FDA Decision Cleared Substantially Equivalent - Third Party Review (ST)
Date Received June 12, 1995
Decision Date August 18, 1995
Days to Decision 67 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 129d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LZH Device Classification - Class 2, Special Controls

Product Code LZH Pump, Infusion, Enteral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 General Hospital devices follow this clearance model.

Regulatory Peers - LZH Pump, Infusion, Enteral

All 12
Devices cleared under the same product code (LZH) and FDA review panel - the closest regulatory comparables to K952671.
Kangaroo Connect Enteral Feeding Pump with Kangaroo Connect Feeding Sets, Kangaroo Connect Portal
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KANGAROO ENTERAL FEEDING SET WITH ENFIT CONNECTORS
K141479 · Covidien · Dec 2014
KANGAROO(R) 524 ENTERAL FEEDING PUMP AND ADMINISTRATION SETS
K945964 · Sherwood Medical Co. · Mar 1995
FLO-GARD 2100 - 2M8281M
K923066 · Baxter Healthcare Corp · May 1993
FLEXIFLO QUANTUM ENTERAL NUTRITION PUMP
K913958 · Abbott Laboratories · Feb 1992