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FDA 510(k)

WHEELCHAIR STUMP SUPPORT

K-Number: K890178 · 1989-09-11

ApplicantGerber Chair Mates, Inc.
Decision Date1989-09-11
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR STUMP SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Gerber Chair Mates, Inc.. It received FDA 510(k) clearance on 1989-09-11 under 510(k) number K890178. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR STUMP SUPPORT?

WHEELCHAIR STUMP SUPPORT is a medical device that received FDA 510(k) clearance on 1989-09-11. The listed applicant is Gerber Chair Mates, Inc.. The 510(k) number is K890178.

When did WHEELCHAIR STUMP SUPPORT receive FDA 510(k) clearance?

WHEELCHAIR STUMP SUPPORT received FDA 510(k) clearance on 1989-09-11, under 510(k) number K890178.

Who is the listed applicant for WHEELCHAIR STUMP SUPPORT?

The FDA 510(k) record lists Gerber Chair Mates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHEELCHAIR STUMP SUPPORT?

The FDA product code for WHEELCHAIR STUMP SUPPORT is KNN.

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Related Devices (Code: KNN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K211919KISS Dynamic Back Support, KISS Dynamic Solid Drop SeatKinetic Innovative Seating System, LLCK942309DYNASTY U1-31 (GELL/CELL)Foley & LardnerK942308DYNASTY GC 12400 (GELL/CELL)Foley & LardnerK942311DYNASTY U1-33 AGMFoley & LardnerK942310DYNASTY GC 12550 (GELL/CELL)Foley & LardnerK942312ALDEN LINEAGE WHEELCHAIR CUSHIONLewis W. Ward

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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