FDA 510(k)

HYDROMASSAGE EQUIP. MODEL 1000

K-Number: K771971 · 1977-10-21

Decision Date1977-10-21

Product CodeILJ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

HYDROMASSAGE EQUIP. MODEL 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Dazey Products Co.. It received FDA 510(k) clearance on 1977-10-21 under 510(k) number K771971. 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 HYDROMASSAGE EQUIP. MODEL 1000?

HYDROMASSAGE EQUIP. MODEL 1000 is a medical device that received FDA 510(k) clearance on 1977-10-21. The listed applicant is Dazey Products Co.. The 510(k) number is K771971.

When did HYDROMASSAGE EQUIP. MODEL 1000 receive FDA 510(k) clearance?

HYDROMASSAGE EQUIP. MODEL 1000 received FDA 510(k) clearance on 1977-10-21, under 510(k) number K771971.

Who is the listed applicant for HYDROMASSAGE EQUIP. MODEL 1000?

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

What is the FDA product code for HYDROMASSAGE EQUIP. MODEL 1000?

The FDA product code for HYDROMASSAGE EQUIP. MODEL 1000 is ILJ.

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Other records listing Dazey Products Co. as applicant

K771969TURBO-JET MODEL 76 K771970WHIRLPOOL BATH MODEL 50 K771966VIBRO BATH MODEL FS-1 K771968WHIRLPOOL BATH MODEL 2273 K771967WHIRLPOOL BATH MODEL 2270

Related Devices (Code: ILJ)

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment AB K052479MBATH 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.