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FDA 510(k)

BATH TUB TRANSFER CHAIR

K-Number: K842649 · 1984-08-10

Decision Date1984-08-10
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BATH TUB TRANSFER CHAIR 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 1984-08-10 under 510(k) number K842649. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATH TUB TRANSFER CHAIR?

BATH TUB TRANSFER CHAIR is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K842649.

When did BATH TUB TRANSFER CHAIR receive FDA 510(k) clearance?

BATH TUB TRANSFER CHAIR received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842649.

Who is the listed applicant for BATH TUB TRANSFER CHAIR?

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 BATH TUB TRANSFER CHAIR?

The FDA product code for BATH TUB TRANSFER CHAIR is IKN.

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: IKN)

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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