Cleared Traditional

K910844 - INFUSION PUMP

K910844 is an FDA 510(k) clearance for INFUSION PUMP, manufactured by Technology Transfer Intl., Inc.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 93-day FDA review.

K910844 · Technology Transfer Intl., Inc. · General Hospital
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May 1991
Decision
93d
Days
Class 2
Risk

K910844 is an FDA 510(k) clearance for the INFUSION PUMP. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Technology Transfer Intl., Inc. (Vienna, US). The FDA issued a Cleared decision on May 31, 1991 after a review of 93 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - the FDA general hospital 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Technology Transfer Intl., Inc. devices

FDA 510(k) Submission Details - K910844

510(k) Number K910844 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 1991
Decision Date May 31, 1991
Days to Decision 93 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 129d · This submission: 93d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 General Hospital devices follow this clearance model.

Regulatory Peers - FRN Pump, Infusion

All 615
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K910844.
AVI MODEL 870 DUAL CHANNEL INFUSION PUMP
K912031 · 3M Avi, Inc. · Jun 1991
RATEMINDER(TM) V INFUSION PUMP, MODIFICATION
K911769 · Critikon Company, LLC · Jun 1991
VOLUMETRIC INFUSION PUMP
K910024 · Baxter Healthcare Corp · May 1991
ABBOTT LIFECARE 5000 PUMP
K911401 · Abbott Laboratories · May 1991
ABBOTT LIFECARE 5000 PUMP MODIFIED
K910919 · Abbott Laboratories · May 1991
EPIDURAL INDICATION FOR BAXTER SYRINGE INFUS PUMP
K911289 · Baxter Healthcare Corp · May 1991