Cleared Traditional

K790879 - ULTIPOR SOLUTION CONTAINER FILTER

K790879 is an FDA 510(k) clearance for ULTIPOR SOLUTION CONTAINER FILTER, manufactured by Pall Biomedical Products Co.. The device is a Class 2 General Hospital device with product code FPB cleared through the Traditional 510(k) pathway after a 25-day FDA review.

K790879 · Pall Biomedical Products Co. · General Hospital
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Jun 1979
Decision
25d
Days
Class 2
Risk

K790879 is an FDA 510(k) clearance for the ULTIPOR SOLUTION CONTAINER FILTER. Classified as Filter, Infusion Line (product code FPB), Class II - Special Controls.

Submitted by Pall Biomedical Products Co. (Walker, US). The FDA issued a Cleared decision on June 1, 1979 after a review of 25 days - a notably fast clearance cycle.

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: 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 Pall Biomedical Products Co. devices

FDA 510(k) Submission Details - K790879

510(k) Number K790879 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 1979
Decision Date June 01, 1979
Days to Decision 25 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
104d faster than avg
Panel avg: 129d · This submission: 25d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPB Device Classification - Class 2, Special Controls

Product Code FPB Filter, Infusion Line
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 - FPB Filter, Infusion Line

All 69
Devices cleared under the same product code (FPB) and FDA review panel - the closest regulatory comparables to K790879.
MICROBAR MONITORING LINE FILTER
K792510 · Medex, Inc. · Dec 1979
BIOGUARD INFUSION LINE FILTER
K791822 · United States Surgical, A Division of Tyco Healthc · Nov 1979
LARGE VOLUME 5 MICRON CONICAL FILTER
K792021 · National Patent Development Corp. · Oct 1979
JELCO* DISC FILTER-0.2 MICRON
K790471 · Jelco Laboratories · Apr 1979
FLUID ADMINISTRATION SETS, 15 MICRON
K790314 · Medex, Inc. · Mar 1979
FILTERSET W/Y-INJECTION SITE, 0.2
K772312 · Abbott Laboratories · Jan 1978