Cleared Traditional

K830772 - TEMP. PACING LEAD

K830772 is an FDA 510(k) clearance for TEMP. PACING LEAD, manufactured by Oscor, Inc.. The device is a Class 2 Cardiovascular device with product code LDF cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K830772 · Oscor, Inc. · Cardiovascular device
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Apr 1983
Decision
38d
Days
Class 2
Risk

K830772 is an FDA 510(k) clearance for the TEMP. PACING LEAD, BIPOLAR #TH60, 90/110. Classified as Electrode, Pacemaker, Temporary (product code LDF), Class II - Special Controls.

Submitted by Oscor, Inc. (Palm Harbor, US). The FDA issued a Cleared decision on April 18, 1983 after a review of 38 days - a notably fast clearance cycle.

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: 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 Oscor, Inc. devices

FDA 510(k) Submission Details - K830772

510(k) Number K830772 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1983
Decision Date April 18, 1983
Days to Decision 38 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
87d faster than avg
Panel avg: 125d · This submission: 38d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LDF Device Classification - Class 2, Special Controls

Product Code LDF Electrode, Pacemaker, Temporary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.3680
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 - LDF Electrode, Pacemaker, Temporary

All 82
Devices cleared under the same product code (LDF) and FDA review panel - the closest regulatory comparables to K830772.
MULTIPOLAR TEMPORARY CARDIAC
K831804 · Oscor, Inc. · Oct 1983
EPCOR MULTIELECTRODE TEMP. PERVENOUS
K832561 · Cordis Corp. · Oct 1983
ELECATH PACEWEDGE DUAL PRESS. BIPOLAR
K832850 · Electro-Catheter Corp. · Oct 1983
USCI TEMP. ATRIO-VENTRICULAR ELECTRODE
K830094 · C.R. Bard, Inc. · Feb 1983
TRANSLUMINAL BIPOLAR PACING PROBE
K813521 · American Edwards Laboratories · Mar 1982
ETHICON* TEMP. CARDIAC PACING WIRE
K813138 · Ethicon, Inc. · Dec 1981