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FDA 510(k)

ELD-ARONDAK CHAIR

K-Number: K926054 · 1993-03-22

ApplicantAl'S Woodcraft, Inc.
Decision Date1993-03-22
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELD-ARONDAK CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Al'S Woodcraft, Inc.. It received FDA 510(k) clearance on 1993-03-22 under 510(k) number K926054. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELD-ARONDAK CHAIR?

ELD-ARONDAK CHAIR is a medical device that received FDA 510(k) clearance on 1993-03-22. The listed applicant is Al'S Woodcraft, Inc.. The 510(k) number is K926054.

When did ELD-ARONDAK CHAIR receive FDA 510(k) clearance?

ELD-ARONDAK CHAIR received FDA 510(k) clearance on 1993-03-22, under 510(k) number K926054.

Who is the listed applicant for ELD-ARONDAK CHAIR?

The FDA 510(k) record lists Al'S Woodcraft, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELD-ARONDAK CHAIR?

The FDA product code for ELD-ARONDAK CHAIR is INM.

Related Clinical Trials

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Related Devices (Code: INM)

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.

K063521NISSIN PEDIATRIC SERIES WHEELCHAIRNissin Medical, Inc.K941738STRYKER 5050 STRECHAIRStryker MedicalK941569CAREMOR CLINERWinco, Inc.K933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAYWinco, Inc.K926028BENCHESTheradapt Products, Inc.K926053ELD-ARONDAK CHAIRAlert Care, 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.

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