Cleared Traditional

K132257 - MANUAL WHEELCHAIR

K132257 is an FDA 510(k) clearance for MANUAL WHEELCHAIR, manufactured by Zhejiang Jiafeng Electrical & Mechanial Co., Ltd.. The device is a Class 1 Physical Medicine device with product code IOR cleared through the Traditional 510(k) pathway after a 209-day FDA review.

K132257 · Zhejiang Jiafeng Electrical & Mechanial Co., Ltd. · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Feb 2014
Decision
209d
Days
Class 1
Risk

K132257 is an FDA 510(k) clearance for the MANUAL WHEELCHAIR. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Zhejiang Jiafeng Electrical & Mechanial Co., Ltd. (Pennington, US). The FDA issued a Cleared decision on February 13, 2014 after a review of 209 days - an extended review cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3850 - the FDA physical medicine 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 Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K132257

510(k) Number K132257 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 2013
Decision Date February 13, 2014
Days to Decision 209 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d slower than avg
Panel avg: 116d · This submission: 209d
Pathway characteristics
Predicate-based equivalence.

IOR Device Classification - Class 1, General Controls

Product Code IOR Wheelchair, Mechanical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3850
Definition A Mechanical Wheelchair Is A Manually Operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And/or Require An Assistive Device For Mobility.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IOR Wheelchair, Mechanical

All 400
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K132257.
TREKKER, TREKKER TRANSIT
K140416 · Convaid Products, Inc. · Sep 2014
VALENTINE STEEL WHEELCHAIR
K130017 · Valentine Intl. , Ltd. · May 2014
EZ TRANSPORT CHAIR
K130517 · Harris Medical, LLC · Feb 2014
BREEZY ELEGANCE
K133855 · Sunrise Medical (Us), LLC · Jan 2014
CAPELLA
K130788 · Future Mobility Healthcare, Inc. · Dec 2013
SHANGHAI PHOENIX MECHANICAL WHEELCHAIR
K130848 · Shanghai Phoenix Medical Equipment Co., Ltd. · Nov 2013
K132257 · MANUAL WHEELCHAIR
Download PDF FDA Summary Zhejiang Jiafeng Elec…