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FDA 510(k)

VANNA BATHING SYSTEM

K-Number: K993872 · 2000-02-16

ApplicantVancare, Inc.
Decision Date2000-02-16
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VANNA BATHING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vancare, Inc.. It received FDA 510(k) clearance on 2000-02-16 under 510(k) number K993872. 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 VANNA BATHING SYSTEM?

VANNA BATHING SYSTEM is a medical device that received FDA 510(k) clearance on 2000-02-16. The listed applicant is Vancare, Inc.. The 510(k) number is K993872.

When did VANNA BATHING SYSTEM receive FDA 510(k) clearance?

VANNA BATHING SYSTEM received FDA 510(k) clearance on 2000-02-16, under 510(k) number K993872.

Who is the listed applicant for VANNA BATHING SYSTEM?

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

What is the FDA product code for VANNA BATHING SYSTEM?

The FDA product code for VANNA BATHING SYSTEM is ILJ.

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.

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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.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner 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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