Nexus Wheelchair Cushion/Formerly Biothotic

FDA 510(k) K923186 · Roho, Inc.

Substantially Equivalent

510(k) numberK923186

Submission

Device name
Nexus Wheelchair Cushion/Formerly Biothotic
Applicant
Roho, Inc.
Belleville, IL, US
Received
June 30, 1992
Decision date
September 9, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KNN – Components, Wheelchair
Device class
Class I (low risk)
Regulation
21 CFR 890.3920
Specialty
Physical Medicine

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K942308Dynasty GC 12400 (Gell/Cell)KNN · Traditional Foley & Lardner11/07/1994SE
K942312Alden Lineage Wheelchair CushionKNN · Traditional Lewis W. Ward05/26/1994SE
K942260Alden Wheelchair CushionKNN · Traditional Ward and Assoc.05/26/1994SE
K933051Zero Gravity Wheelchair Components, ModificationKNN · Traditional General Components Intl., Inc.10/12/1993SE
K925980PMKNN · Traditional Pathfinder Intl. Corp.03/24/1993SE
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Questions and answers

When was Nexus Wheelchair Cushion/Formerly Biothotic cleared by the FDA?

Nexus Wheelchair Cushion/Formerly Biothotic (K923186) received a 510(k) decision of Substantially Equivalent on September 9, 1992, 71 days after the submission was received.

What is the product code of K923186?

The FDA product code is KNN – Components, Wheelchair, a Class I (low risk) device regulated under 21 CFR 890.3920.