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FDA 510(k)

WHIRLPOOL BATHING UNIT-#2001

K-Number: K802335 · 1980-10-10

ApplicantAqua Care Corp.
Decision Date1980-10-10
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHIRLPOOL BATHING UNIT-#2001 is the device name listed in this FDA 510(k) record. The listed applicant is Aqua Care Corp.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802335. 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 WHIRLPOOL BATHING UNIT-#2001?

WHIRLPOOL BATHING UNIT-#2001 is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Aqua Care Corp.. The 510(k) number is K802335.

When did WHIRLPOOL BATHING UNIT-#2001 receive FDA 510(k) clearance?

WHIRLPOOL BATHING UNIT-#2001 received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802335.

Who is the listed applicant for WHIRLPOOL BATHING UNIT-#2001?

The FDA 510(k) record lists Aqua Care Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHIRLPOOL BATHING UNIT-#2001?

The FDA product code for WHIRLPOOL BATHING UNIT-#2001 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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