Cleared Traditional

K960321 - CARDIOCATH CATHETERIZATION LAB SYSTEM

K960321 is an FDA 510(k) clearance for CARDIOCATH CATHETERIZATION LAB SYSTEM, manufactured by Prucka Engineering, Inc.. The device is a Class 2 Cardiovascular device with product code DPS cleared through the Traditional 510(k) pathway after a 212-day FDA review.

K960321 · Prucka Engineering, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1996
Decision
212d
Days
Class 2
Risk

K960321 is an FDA 510(k) clearance for the CARDIOCATH CATHETERIZATION LAB SYSTEM. Classified as Electrocardiograph (product code DPS), Class II - Special Controls.

Submitted by Prucka Engineering, Inc. (Houston, US). The FDA issued a Cleared decision on August 21, 1996 after a review of 212 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2340 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Prucka Engineering, Inc. devices

FDA 510(k) Submission Details - K960321

510(k) Number K960321 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 1996
Decision Date August 21, 1996
Days to Decision 212 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
87d slower than avg
Panel avg: 125d · This submission: 212d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPS Device Classification - Class 2, Special Controls

Product Code DPS Electrocardiograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2340
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 - DPS Electrocardiograph

All 401
Devices cleared under the same product code (DPS) and FDA review panel - the closest regulatory comparables to K960321.
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