Cleared Traditional

K880932 - MRL PACETTE

K880932 is an FDA 510(k) clearance for MRL PACETTE, manufactured by Medical Research Laboratories, Inc.. The device is a Class 2 Cardiovascular device with product code DRO cleared through the Traditional 510(k) pathway after a 284-day FDA review.

K880932 · Medical Research Laboratories, Inc. · Cardiovascular device
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Dec 1988
Decision
284d
Days
Class 2
Risk

K880932 is an FDA 510(k) clearance for the MRL PACETTE, 450SLL. Classified as Pacemaker, Cardiac, External Transcutaneous (non-invasive) (product code DRO), Class II - Special Controls.

Submitted by Medical Research Laboratories, Inc. (Niles, US). The FDA issued a Cleared decision on December 16, 1988 after a review of 284 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5550 - 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 Medical Research Laboratories, Inc. devices

FDA 510(k) Submission Details - K880932

510(k) Number K880932 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 1988
Decision Date December 16, 1988
Days to Decision 284 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
159d slower than avg
Panel avg: 125d · This submission: 284d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DRO Device Classification - Class 2, Special Controls

Product Code DRO Pacemaker, Cardiac, External Transcutaneous (non-invasive)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5550
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 - DRO Pacemaker, Cardiac, External Transcutaneous (non-invasive)

All 41
Devices cleared under the same product code (DRO) and FDA review panel - the closest regulatory comparables to K880932.
NKA MODEL SEC-3102 CARDIAC STIMULATOR
K894492 · Nihon Kohden America, Inc. · Dec 1989
DEFIB/PACING PADS
K894588 · Conmedcorp · Oct 1989
MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
K885171 · Andover Medical, Inc. · Jan 1989
TRIAD-EP II, PUSHBUTTON, CABLE INPUT
K884532 · Cardiotronics, Inc. · Nov 1988
TRIAD-EP II, PLATE INPUT
K884530 · Cardiotronics, Inc. · Nov 1988
TRIAD-EP, PUSHBUTTON, CABLE INPUT TYPE
K883178 · Cardiotronics, Inc. · Nov 1988