Cleared Traditional

K791490 - UNIPUNCTURE CATHETER

K791490 is the FDA 510(k) clearance for UNIPUNCTURE CATHETER by Hospal Medical Corp.. It is a Class 2 Gastroenterology & Urology device (product code FIE) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K791490 · Hospal Medical Corp. · Gastroenterology & Urology device
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Oct 1979
Decision
84d
Days
Class 2
Risk

K791490 is an FDA 510(k) clearance for the UNIPUNCTURE CATHETER. Classified as Needle, Fistula (product code FIE), Class II - Special Controls.

Submitted by Hospal Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on October 26, 1979 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5540 - 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 Hospal Medical Corp. devices

Submission Details

510(k) Number K791490 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 03, 1979
Decision Date October 26, 1979
Days to Decision 84 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
46d faster than avg
Panel avg: 130d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FIE Needle, Fistula
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5540
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 - FIE Needle, Fistula

All 21
Devices cleared under the same product code (FIE) and FDA review panel - the closest regulatory comparables to K791490.
HEMO-CATH II KIDNEY DIALYSIS CATHETER
K801966 · Medical Components, Inc. · Sep 1980
ARGYLE A-V MEDI-WING HEMODIALYSIS SET
K801618 · Sherwood Medical Co. · Aug 1980
VITAL CATHETER
K791489 · Hospal Medical Corp. · Oct 1979
A.V. FISTULA NEEDLE SET
K782021 · Cordis Corp. · Mar 1979
A.V. FISTULA NEEDLE SET (#344)
K771490 · Sorensen Research · Aug 1977
A.V. FISTULA NEEDLE SET (#364)
K771491 · Sorensen Research · Aug 1977