Cleared Traditional

K982099 - MOMENTUM NO. FS008 WHEELCHAIR

K982099 is an FDA 510(k) clearance for MOMENTUM NO. FS008 WHEELCHAIR, manufactured by Sriram Enterprises D.B.A. Momentum Group. The device is a Class 1 Physical Medicine device with product code IOR cleared through the Traditional 510(k) pathway after a 112-day FDA review.

K982099 · Sriram Enterprises D.B.A. Momentum Group · Physical Medicine device
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Optimized for regulatory review, auditing and printing
Oct 1998
Decision
112d
Days
Class 1
Risk

K982099 is an FDA 510(k) clearance for the MOMENTUM NO. FS008 WHEELCHAIR. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Sriram Enterprises D.B.A. Momentum Group (Orlando, US). The FDA issued a Cleared decision on October 5, 1998 after a review of 112 days - within the typical 510(k) review window.

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.

View all Sriram Enterprises D.B.A. Momentum Group devices

FDA 510(k) Submission Details - K982099

510(k) Number K982099 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 15, 1998
Decision Date October 05, 1998
Days to Decision 112 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
3d faster than avg
Panel avg: 115d · This submission: 112d
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 138
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K982099.
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