Cleared Traditional

K891062 - TERUMO AV FISTULA NEEDLE SET

K891062 is an FDA 510(k) clearance for TERUMO AV FISTULA NEEDLE SET, manufactured by Terumo Medical Corp.. The device is a Class 2 Gastroenterology & Urology device with product code FIE cleared through the Traditional 510(k) pathway after a 113-day FDA review.

K891062 · Terumo Medical Corp. · Gastroenterology & Urology device
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Jun 1989
Decision
113d
Days
Class 2
Risk

K891062 is an FDA 510(k) clearance for the TERUMO AV FISTULA NEEDLE SET. Classified as Needle, Fistula (product code FIE), Class II - Special Controls.

Submitted by Terumo Medical Corp. (Elkton, US). The FDA issued a Cleared decision on June 22, 1989 after a review of 113 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Terumo Medical Corp. devices

FDA 510(k) Submission Details - K891062

510(k) Number K891062 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 01, 1989
Decision Date June 22, 1989
Days to Decision 113 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
17d faster than avg
Panel avg: 130d · This submission: 113d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FIE Device Classification - Class 2, Special Controls

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 40
Devices cleared under the same product code (FIE) and FDA review panel - the closest regulatory comparables to K891062.
JMS APHERESIS NEEDLE
K915174 · Jms Co., Ltd. · Mar 1993
JMS AV FISTULA NEEDLES
K911199 · Jms Co., Ltd. · Aug 1991
ARTERIOVENOUS FISTULA SETS
K900125 · Baxter Healthcare Corp · Jan 1990
JMS APHERESIS NEEDLE
K880726 · Jms Co., Ltd. · Mar 1988
JMD AV FISTULA NEEDLE (MODIFICATION)
K860789 · Jms Co., Ltd. · Mar 1986
JMS AV FISTULA NEEDLE
K860241 · Jms Co., Ltd. · Feb 1986