Cleared Traditional

K800838 - ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.

K800838 is an FDA 510(k) clearance for ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN., manufactured by Arco Medical Products Co.. The device is a Class 3 Cardiovascular device with product code DXY cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K800838 · Arco Medical Products Co. · Cardiovascular device
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Jun 1980
Decision
50d
Days
Class 3
Risk

K800838 is an FDA 510(k) clearance for the ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Arco Medical Products Co. (Mchenry, US). The FDA issued a Cleared decision on June 4, 1980 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3610 - 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: High-complexity regulatory submission. High regulatory complexity profile. 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 Arco Medical Products Co. devices

FDA 510(k) Submission Details - K800838

510(k) Number K800838 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1980
Decision Date June 04, 1980
Days to Decision 50 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
75d faster than avg
Panel avg: 125d · This submission: 50d
Pathway characteristics
Predicate-based equivalence.

DXY Device Classification - Class 3, Premarket Approval

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - DXY Implantable Pacemaker Pulse-generator

All 388
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K800838.
MICROTHIN-D1 (MOD. 0620)
K801122 · Cardiac Pacemakers, Inc. · Jun 1980
UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.
K801241 · Arco Medical Products Co. · Jun 1980
MEDTRONIC MODELS 5966/5967, ETC.
K800069 · Medtronic Vascular · Jun 1980
MODEL 5985 PACEMAKER PULSE GENERATOR
K800285 · Medtronic Vascular · May 1980
PULSE GENERATORS MODELS 657 & 677
K800387 · Siemens Elema AB · May 1980
MODEL 253-11 CYBERLITH PULSE GENERATOR
K800895 · Intermedics, Inc. · Apr 1980