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FDA 510(k)

THE ERGOSYSTEM CHAIR

K-Number: K863728 · 1986-10-31

ApplicantCharles D. Bell, Inc.
Decision Date1986-10-31
Product CodeHME
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE ERGOSYSTEM CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Charles D. Bell, Inc.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863728. The device is classified under product code HME. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ERGOSYSTEM CHAIR?

THE ERGOSYSTEM CHAIR is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Charles D. Bell, Inc.. The 510(k) number is K863728.

When did THE ERGOSYSTEM CHAIR receive FDA 510(k) clearance?

THE ERGOSYSTEM CHAIR received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863728.

Who is the listed applicant for THE ERGOSYSTEM CHAIR?

The FDA 510(k) record lists Charles D. Bell, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ERGOSYSTEM CHAIR?

The FDA product code for THE ERGOSYSTEM CHAIR is HME.

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Related Devices (Code: HME)

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.

K930449MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIRMarco Ophthalmic, Inc.K914416BREATH-EASY, MODIFICATIONIcor ABK894018RELIANCE(R) 6200 EXAMINATION CHAIRReliance Medical Products, Inc.K870112STORZ ENT/OPHTHALMIC MAXI CHAIRStorz Instrument Co.K864494MODEL 6500 OPTHALMIC CHAIRKoken Mfg Company, Inc.K864574MAC 150E OPTHALMIC CHAIRKoken Mfg Company, Inc.

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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