Cleared Traditional

K902716 - PE ELECTROPHYSIOLOGY LAB SYSTEM (PEEP)

K902716 is an FDA 510(k) clearance for PE ELECTROPHYSIOLOGY LAB SYSTEM (PEEP), manufactured by Prucka Engineering, Inc.. The device is a Class 2 Cardiovascular device with product code DQK cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K902716 · Prucka Engineering, Inc. · Cardiovascular device
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Sep 1990
Decision
76d
Days
Class 2
Risk

K902716 is an FDA 510(k) clearance for the PE ELECTROPHYSIOLOGY LAB SYSTEM (PEEP). Classified as Computer, Diagnostic, Programmable (product code DQK), Class II - Special Controls.

Submitted by Prucka Engineering, Inc. (Houston, US). The FDA issued a Cleared decision on September 4, 1990 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1425 - 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 Prucka Engineering, Inc. devices

FDA 510(k) Submission Details - K902716

510(k) Number K902716 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 20, 1990
Decision Date September 04, 1990
Days to Decision 76 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 125d · This submission: 76d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQK Device Classification - Class 2, Special Controls

Product Code DQK Computer, Diagnostic, Programmable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1425
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 - DQK Computer, Diagnostic, Programmable

All 361
Devices cleared under the same product code (DQK) and FDA review panel - the closest regulatory comparables to K902716.
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