Cleared Traditional

K820676 - TOUCH FLUSH W/Y TRANSDUCER CONNECTOR

K820676 is the FDA 510(k) clearance for TOUCH FLUSH W/Y TRANSDUCER CONNECTOR by Norton Performance Plastics Corp.. It is a Class 2 Cardiovascular device (product code DRS) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K820676 · Norton Performance Plastics Corp. · Cardiovascular device
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Mar 1982
Decision
14d
Days
Class 2
Risk

K820676 is an FDA 510(k) clearance for the TOUCH FLUSH W/Y TRANSDUCER CONNECTOR. Classified as Transducer, Blood-pressure, Extravascular (product code DRS), Class II - Special Controls.

Submitted by Norton Performance Plastics Corp. (Walker, US). The FDA issued a Cleared decision on March 25, 1982 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2850 - 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 Norton Performance Plastics Corp. devices

Submission Details

510(k) Number K820676 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1982
Decision Date March 25, 1982
Days to Decision 14 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
111d faster than avg
Panel avg: 125d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DRS Transducer, Blood-pressure, Extravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2850
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 - DRS Transducer, Blood-pressure, Extravascular

All 70
Devices cleared under the same product code (DRS) and FDA review panel - the closest regulatory comparables to K820676.
DISPOSABLE TRANSDUCER DOMES & KITS
K821894 · American Pharmaseal Div. Ahsc · Jul 1982
DISPOSABLE BLOOD PRESSURE TRANSDUCER
K821416 · Bentley Laboratories, Inc. · Jul 1982
FLEX-E1 ECG ELECTRODE
K820579 · Conmedcorp · Apr 1982
TOUCH FLUSH CONTINUOUS FAST/FLUSH
K820677 · Norton Performance Plastics Corp. · Mar 1982
MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS
K820457 · Graphic Controls Corp. · Mar 1982
PHYSIOLOGICAL PRESSURE TRANSDUCER #900
K820342 · Bentley Laboratories, Inc. · Mar 1982