Cleared Traditional

K851048 - CHEST CATHETERS/THORACIC CATHETERS

K851048 is the FDA 510(k) clearance for CHEST CATHETERS/THORACIC CATHETERS by Medovations, Inc.. It is a Class 1 General & Plastic Surgery device (product code GBS) cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K851048 · Medovations, Inc. · General & Plastic Surgery device
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Jun 1985
Decision
83d
Days
Class 1
Risk

K851048 is an FDA 510(k) clearance for the CHEST CATHETERS/THORACIC CATHETERS. Classified as Catheter, Ventricular, General & Plastic Surgery (product code GBS), Class I - General Controls.

Submitted by Medovations, Inc. (Wauwatosa, US). The FDA issued a Cleared decision on June 5, 1985 after a review of 83 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4200 - the FDA general and plastic surgery device 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 Medovations, Inc. devices

Submission Details

510(k) Number K851048 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 14, 1985
Decision Date June 05, 1985
Days to Decision 83 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 115d · This submission: 83d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GBS Catheter, Ventricular, General & Plastic Surgery
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - GBS Catheter, Ventricular, General & Plastic Surgery

All 11
Devices cleared under the same product code (GBS) and FDA review panel - the closest regulatory comparables to K851048.
URESIL STD FLAT/ROUND & FLAT/ROUND SPLIT. SILI/DRA
K863560 · Uresil Corp. · Sep 1986
THORACIC CATHETER (CHEST DRAINAGE TUBE)
K863142 · Sheridan Catheter Corp. · Aug 1986
OSTEOTOMY DRAINAGE TUBE
K862584 · Treace Medical, Inc. · Aug 1986
ARGYLE MEDIASTINAL DRAIN
K822318 · Sherwood Medical Co. · Aug 1982
SIL-V-UR CHEST CATHETER
K813463 · C.R. Bard, Inc. · Feb 1982
DAVOL SILICONE SHEATH SUMP DRAIN
K810158 · C.R. Bard, Inc. · Feb 1981