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FDA 510(k)

FREEDOM BATH

K-Number: K952442 · 1995-11-02

ApplicantGrand Traverse Technologies
Decision Date1995-11-02
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FREEDOM BATH is the device name listed in this FDA 510(k) record. The listed applicant is Grand Traverse Technologies. It received FDA 510(k) clearance on 1995-11-02 under 510(k) number K952442. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM BATH?

FREEDOM BATH is a medical device that received FDA 510(k) clearance on 1995-11-02. The listed applicant is Grand Traverse Technologies. The 510(k) number is K952442.

When did FREEDOM BATH receive FDA 510(k) clearance?

FREEDOM BATH received FDA 510(k) clearance on 1995-11-02, under 510(k) number K952442.

Who is the listed applicant for FREEDOM BATH?

The FDA 510(k) record lists Grand Traverse Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEDOM BATH?

The FDA product code for FREEDOM BATH is ILJ.

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Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, 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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