Cleared Traditional

K820987 - FOLEY INSERTION TRAYS W/OVERWRAY

K820987 is the FDA 510(k) clearance for FOLEY INSERTION TRAYS W/OVERWRAY by Inmed Corp.. It is a Class 2 Gastroenterology & Urology device (product code KOD) cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K820987 · Inmed Corp. · Gastroenterology & Urology device
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May 1982
Decision
36d
Days
Class 2
Risk

K820987 is an FDA 510(k) clearance for the FOLEY INSERTION TRAYS W/OVERWRAY. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Inmed Corp. (Mchenry, US). The FDA issued a Cleared decision on May 13, 1982 after a review of 36 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 Inmed Corp. devices

Submission Details

510(k) Number K820987 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1982
Decision Date May 13, 1982
Days to Decision 36 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
94d faster than avg
Panel avg: 130d · This submission: 36d
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 120
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K820987.
DYNACOR URETHRAL CATHETER TRAY
K821970 · Medline Industries, Inc. · Jul 1982
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
URETERAL CATHETER CONNECTING TUBE
K820866 · Van-Tec, Inc. · Apr 1982
URETERAL CATHETER CONNECTOR
K820868 · Van-Tec, Inc. · Apr 1982