Cleared Traditional

K811910 - VEIN-TRAP TM

K811910 is an FDA 510(k) clearance for VEIN-TRAP TM, manufactured by Atrium Medical Corp.. The device is a Class 2 Cardiovascular device with product code DWQ cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K811910 · Atrium Medical Corp. · Cardiovascular device
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Jul 1981
Decision
19d
Days
Class 2
Risk

K811910 is an FDA 510(k) clearance for the VEIN-TRAP TM. Classified as Stripper, Vein, External (product code DWQ), Class II - Special Controls.

Submitted by Atrium Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on July 20, 1981 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4885 - the FDA cardiovascular device oversight 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 Atrium Medical Corp. devices

FDA 510(k) Submission Details - K811910

510(k) Number K811910 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1981
Decision Date July 20, 1981
Days to Decision 19 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
106d faster than avg
Panel avg: 125d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DWQ Device Classification - Class 2, Special Controls

Product Code DWQ Stripper, Vein, External
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4885
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.