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FDA 510(k)

COMMODE CHAIR 98200

K-Number: K842651 · 1984-08-07

Decision Date1984-08-07
Product CodeILS
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMMODE CHAIR 98200 is the device name listed in this FDA 510(k) record. The listed applicant is Guardian Products Co., Inc.. It received FDA 510(k) clearance on 1984-08-07 under 510(k) number K842651. The device is classified under product code ILS. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMMODE CHAIR 98200?

COMMODE CHAIR 98200 is a medical device that received FDA 510(k) clearance on 1984-08-07. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K842651.

When did COMMODE CHAIR 98200 receive FDA 510(k) clearance?

COMMODE CHAIR 98200 received FDA 510(k) clearance on 1984-08-07, under 510(k) number K842651.

Who is the listed applicant for COMMODE CHAIR 98200?

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

What is the FDA product code for COMMODE CHAIR 98200?

The FDA product code for COMMODE CHAIR 98200 is ILS.

Related Clinical Trials

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.

Other records listing Guardian Products Co., Inc. as applicant

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.

View all 8 devices →

Related Devices (Code: ILS)

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.

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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