FDA 510(k)

WHEELCHAIR MUFF

K-Number: K780195 · 1978-03-09

Decision Date1978-03-09

Product CodeKNO

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR MUFF is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-03-09 under 510(k) number K780195. The device is classified under product code KNO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR MUFF?

WHEELCHAIR MUFF is a medical device that received FDA 510(k) clearance on 1978-03-09. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K780195.

When did WHEELCHAIR MUFF receive FDA 510(k) clearance?

WHEELCHAIR MUFF received FDA 510(k) clearance on 1978-03-09, under 510(k) number K780195.

Who is the listed applicant for WHEELCHAIR MUFF?

The FDA 510(k) record lists Orthopedic Equipment Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHEELCHAIR MUFF?

The FDA product code for WHEELCHAIR MUFF is KNO.

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Other records listing Orthopedic Equipment Co., Inc. as applicant

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COM K841189OEC/REZAIAN SPINAL FIXATOR K800530SCHLEIN TRI-SURFACE ANKLE K781445SPREADER K790247TOURNIQUET TEST GAGE K790209FILTER SYSTEM, ALTNER DISPOSABLE

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Related Devices (Code: KNO)

K870298REDMAN ACCESSORIESRedman, Inc.K823646FRICTION FEEDERFred Sammons, Inc.K823645VELCRO STRAPS TO HOLD ARM TO WHEELCHAIRFred Sammons, Inc.K823816WHEELCHAIR PATIENT RESTRAINTSDanek Medical, Inc.K823635CUSHIONS FOR WHEELCHAIR ARMSFred Sammons, Inc.K823636ARM THROUGH FOR WHEELCHAIR BK-6459-01 &Fred Sammons, Inc.

Official Source

View on FDA Database →

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