Cleared Traditional

K221327 - BD Alaris Pump Infusion Sets

K221327 is the FDA 510(k) clearance for BD Alaris Pump Infusion Sets by Care Fusion. It is a Class 2 General Hospital device (product code FPA) cleared through the Traditional 510(k) pathway after a 441-day FDA review.

K221327 · Care Fusion · General Hospital
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Optimized for regulatory review, auditing and printing
Jul 2023
Decision
441d
Days
Class 2
Risk

K221327 is an FDA 510(k) clearance for the BD Alaris™ Pump Infusion Sets. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Care Fusion (San Diego, US). The FDA issued a Cleared decision on July 21, 2023 after a review of 441 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General Hospital submissions.

View all Care Fusion devices

Submission Details

510(k) Number K221327 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2022
Decision Date July 21, 2023
Days to Decision 441 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
312d slower than avg
Panel avg: 129d · This submission: 441d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FPA Set, Administration, Intravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - FPA Set, Administration, Intravascular

All 445
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