Cleared Traditional

K810894 - FOGARTY FLEXIBLE CALIBRATOR

K810894 is the FDA 510(k) clearance for FOGARTY FLEXIBLE CALIBRATOR by American Edwards Laboratories. It is a Class 2 Cardiovascular device (product code DWP) cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K810894 · American Edwards Laboratories · Cardiovascular device
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May 1981
Decision
42d
Days
Class 2
Risk

K810894 is an FDA 510(k) clearance for the FOGARTY FLEXIBLE CALIBRATOR. Classified as Dilator, Vessel, Surgical (product code DWP), Class II - Special Controls.

Submitted by American Edwards Laboratories (Mchenry, US). The FDA issued a Cleared decision on May 15, 1981 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4475 - 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 American Edwards Laboratories devices

Submission Details

510(k) Number K810894 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 1981
Decision Date May 15, 1981
Days to Decision 42 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
83d faster than avg
Panel avg: 125d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DWP Dilator, Vessel, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4475
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.

Regulatory Peers - DWP Dilator, Vessel, Surgical

All 9
Devices cleared under the same product code (DWP) and FDA review panel - the closest regulatory comparables to K810894.
VESSEL DILATOR
K832595 · Abbott Laboratories · Aug 1983
REUSABLE FOGARTY FLEXIBLE CALIBRATOR
K822687 · American Edwards Laboratories · Oct 1982
FOGARTY FLEXIBLE PROBE
K812935 · American Edwards Laboratories · Nov 1981
BONCHEK-SHILEY VEIN DISTENTION SYSTEM
K792134 · Shiley, Inc. · Dec 1979
SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO
K790938 · Shiley, Inc. · Jun 1979