Cleared Traditional

K813587 - DISPOSABLE THORACIC CATHETER

K813587 is the FDA 510(k) clearance for DISPOSABLE THORACIC CATHETER by Texas Medical Products, Inc.. It is a Class 1 General & Plastic Surgery device (product code GBS) cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K813587 · Texas Medical Products, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1982
Decision
15d
Days
Class 1
Risk

K813587 is an FDA 510(k) clearance for the DISPOSABLE THORACIC CATHETER. Classified as Catheter, Ventricular, General & Plastic Surgery (product code GBS), Class I - General Controls.

Submitted by Texas Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 12, 1982 after a review of 15 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 Texas Medical Products, Inc. devices

Submission Details

510(k) Number K813587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1981
Decision Date January 12, 1982
Days to Decision 15 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
100d faster than avg
Panel avg: 115d · This submission: 15d
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 K813587.
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
ARGYLE SILICONE THORACIC CATHETER
K802318 · Sherwood Medical Co. · Oct 1980