Cleared Traditional

K821970 - DYNACOR URETHRAL CATHETER TRAY

K821970 is the FDA 510(k) clearance for DYNACOR URETHRAL CATHETER TRAY by Medline Industries, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KOD) cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K821970 · Medline Industries, Inc. · Gastroenterology & Urology device
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Jul 1982
Decision
20d
Days
Class 2
Risk

K821970 is an FDA 510(k) clearance for the DYNACOR URETHRAL CATHETER TRAY. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Medline Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 21, 1982 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5130 - the FDA gastroenterology and urology 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 Medline Industries, Inc. devices

Submission Details

510(k) Number K821970 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1982
Decision Date July 21, 1982
Days to Decision 20 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 130d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KOD Catheter, Urological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5130
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - KOD Catheter, Urological

All 115
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K821970.
URETERAL STONE EXTRACTOR CATHETER
K831244 · American Edwards Laboratories · Jun 1983
STERILE, ALL PURPOSE URETHRAL CATHETER
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CATHETER HOLDER
K823818 · Danek Medical, Inc. · Jan 1983
BARDEX ALL SILICONE PEDIATRIC CATHETER
K821745 · C.R. Bard, Inc. · Jun 1982
BN-74 COATED BARDEX ALL SILICONE CATH
K821272 · C.R. Bard, Inc. · Jun 1982
CURITY ECONOMY I CYSTOSCOPY
K820838 · The Kendal Co. · May 1982