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FDA 510(k)

BATHTUB TRANSFER BENCH

K-Number: K821010 · 1982-04-21

Decision Date1982-04-21
Product CodeIKX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BATHTUB TRANSFER BENCH 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 1982-04-21 under 510(k) number K821010. The device is classified under product code IKX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATHTUB TRANSFER BENCH?

BATHTUB TRANSFER BENCH is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Guardian Products Co., Inc.. The 510(k) number is K821010.

When did BATHTUB TRANSFER BENCH receive FDA 510(k) clearance?

BATHTUB TRANSFER BENCH received FDA 510(k) clearance on 1982-04-21, under 510(k) number K821010.

Who is the listed applicant for BATHTUB TRANSFER BENCH?

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 BATHTUB TRANSFER BENCH?

The FDA product code for BATHTUB TRANSFER BENCH is IKX.

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: IKX)

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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