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FDA 510(k)

WHIRLPOOL BATH MODEL 2274

K-Number: K771965 · 1977-10-28

ApplicantDozey Products Co.
Decision Date1977-10-28
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHIRLPOOL BATH MODEL 2274 is the device name listed in this FDA 510(k) record. The listed applicant is Dozey Products Co.. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K771965. 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 BATH MODEL 2274?

WHIRLPOOL BATH MODEL 2274 is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is Dozey Products Co.. The 510(k) number is K771965.

When did WHIRLPOOL BATH MODEL 2274 receive FDA 510(k) clearance?

WHIRLPOOL BATH MODEL 2274 received FDA 510(k) clearance on 1977-10-28, under 510(k) number K771965.

Who is the listed applicant for WHIRLPOOL BATH MODEL 2274?

The FDA 510(k) record lists Dozey Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHIRLPOOL BATH MODEL 2274?

The FDA product code for WHIRLPOOL BATH MODEL 2274 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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