Cleared Traditional

K782046 - C-CORD

K782046 is an FDA 510(k) clearance for C-CORD, manufactured by Concept, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FFZ cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K782046 · Concept, Inc. · Gastroenterology & Urology device
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Jan 1979
Decision
33d
Days
Class 2
Risk

K782046 is an FDA 510(k) clearance for the C-CORD. Classified as Cord, Electric, For Endoscope (product code FFZ), Class II - Special Controls.

Submitted by Concept, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 10, 1979 after a review of 33 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - 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 Concept, Inc. devices

FDA 510(k) Submission Details - K782046

510(k) Number K782046 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1978
Decision Date January 10, 1979
Days to Decision 33 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
97d faster than avg
Panel avg: 130d · This submission: 33d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FFZ Device Classification - Class 2, Special Controls

Product Code FFZ Cord, Electric, For Endoscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
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.