Cleared Traditional

K823895 - MODEL RF. D&RX..D PACEMAKER LEADS

K823895 is an FDA 510(k) clearance for MODEL RF. D&RX..D PACEMAKER LEADS, manufactured by Oscor, Inc.. The device is a Class 3 Cardiovascular device with product code DTB cleared through the Traditional 510(k) pathway after a 124-day FDA review.

K823895 · Oscor, Inc. · Cardiovascular device
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Apr 1983
Decision
124d
Days
Class 3
Risk

K823895 is an FDA 510(k) clearance for the MODEL RF. D&RX..D PACEMAKER LEADS. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Oscor, Inc. (Palm Harbor, US). The FDA issued a Cleared decision on April 30, 1983 after a review of 124 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3680 - 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 Oscor, Inc. devices

FDA 510(k) Submission Details - K823895

510(k) Number K823895 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1982
Decision Date April 30, 1983
Days to Decision 124 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
1d faster than avg
Panel avg: 125d · This submission: 124d
Pathway characteristics
Predicate-based equivalence.

DTB Device Classification - Class 3, Premarket Approval

Product Code DTB Permanent Pacemaker Electrode
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3680
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 - DTB Permanent Pacemaker Electrode

All 396
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K823895.
POROUS TIP ENDOCARDIAL LEAD
K830743 · Daig Corp. · May 1983
MODEL JY PACEMAKER LEAD - VARIOUS
K823889 · Oscor, Inc. · Apr 1983
MODEL MZ PACEMAKER LEAD-VARIOUS
K823893 · Oscor, Inc. · Apr 1983
MODEL SF. D&SX.D PACEMAKER LEADS
K823897 · Oscor, Inc. · Apr 1983
MODEL MF..D & MX..D PACEMAKER LEADS
K823898 · Oscor, Inc. · Apr 1983
IMPLANTABLE PACING LEAD CCS MODEL SV-101
K830828 · Cardiac Control Systems, Inc. · Apr 1983