Cleared Traditional

K901884 - 7620 REMOTE CENTRAL STATION REPEATER

K901884 is the FDA 510(k) clearance for 7620 REMOTE CENTRAL STATION REPEATER by Marquette Electronics, Inc.. It is a Class 2 Cardiovascular device (product code DXJ) cleared through the Traditional 510(k) pathway after a 47-day FDA review.

K901884 · Marquette Electronics, Inc. · Cardiovascular device
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Jun 1990
Decision
47d
Days
Class 2
Risk

K901884 is an FDA 510(k) clearance for the 7620 REMOTE CENTRAL STATION REPEATER. Classified as Display, Cathode-ray Tube, Medical (product code DXJ), Class II - Special Controls.

Submitted by Marquette Electronics, Inc. (Milwaukee, US). The FDA issued a Cleared decision on June 12, 1990 after a review of 47 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2450 - 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 Marquette Electronics, Inc. devices

Submission Details

510(k) Number K901884 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 26, 1990
Decision Date June 12, 1990
Days to Decision 47 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
78d faster than avg
Panel avg: 125d · This submission: 47d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DXJ Display, Cathode-ray Tube, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2450
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 - DXJ Display, Cathode-ray Tube, Medical

All 56
Devices cleared under the same product code (DXJ) and FDA review panel - the closest regulatory comparables to K901884.
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CENTRALSCOPE 12
K901072 · Marquette Electronics, Inc. · Aug 1990
HORIZON DISPLAY CONTROLLER PART # 266-200-010
K884423 · Mennen Medical, Inc. · May 1989
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K883973 · Nihon Kohden America, Inc. · Nov 1988
Q-CATH RM
K883031 · Quinton, Inc. · Sep 1988