Cleared Traditional

K940073 - EXTENSION TUBE, EXTENSION TUBE LENGTH 20, & 30

K940073 is an FDA 510(k) clearance for EXTENSION TUBE, manufactured by Puritas Health Care, Inc.. The device is a Class 2 General Hospital device with product code FPA cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K940073 · Puritas Health Care, Inc. · General Hospital
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Mar 1994
Decision
76d
Days
Class 2
Risk

K940073 is an FDA 510(k) clearance for the EXTENSION TUBE, EXTENSION TUBE LENGTH 20, & 30. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Puritas Health Care, Inc. (New Milford, US). The FDA issued a Cleared decision on March 23, 1994 after a review of 76 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 Puritas Health Care, Inc. devices

FDA 510(k) Submission Details - K940073

510(k) Number K940073 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 1994
Decision Date March 23, 1994
Days to Decision 76 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 129d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPA Device Classification - Class 2, Special Controls

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 620
Devices cleared under the same product code (FPA) and FDA review panel - the closest regulatory comparables to K940073.
LIFECARE PLUMSET VENTED SECONDARY I.V. SET
K933326 · Abbott Laboratories · Mar 1994
INFUSION ADMINISTRATION SET
K940053 · Puritas Health Care, Inc. · Mar 1994
I.V. SET (20 DROPS/ML)
K940072 · Puritas Health Care, Inc. · Mar 1994
SAFE CONNECTOR
K940296 · Icu Medical, Inc. · Feb 1994
REMOTE RESERVOIR ADAPTER(TM) CASSETTE WITH BAG
K933390 · Pharmacia Deltec, Inc. · Feb 1994
0.22 MICRON FINAL FILTER WITH EXTENSION TUBE
K935601 · Puritas Health Care, Inc. · Jan 1994