Cleared Traditional

K123822 - KLEIN TOUCH PUMP AND DISPOSABLE TUBING SET

K123822 is an FDA 510(k) clearance for KLEIN TOUCH PUMP AND DISPOSABLE TUBING SET, manufactured by Hk Surgical, Inc.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 289-day FDA review.

K123822 · Hk Surgical, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2013
Decision
289d
Days
Class 2
Risk

K123822 is an FDA 510(k) clearance for the KLEIN TOUCH PUMP AND DISPOSABLE TUBING SET. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Hk Surgical, Inc. (San Clemente, US). The FDA issued a Cleared decision on September 27, 2013 after a review of 289 days - an extended review cycle.

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 Hk Surgical, Inc. devices

FDA 510(k) Submission Details - K123822

510(k) Number K123822 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 12, 2012
Decision Date September 27, 2013
Days to Decision 289 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
160d slower than avg
Panel avg: 129d · This submission: 289d
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 500
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