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FDA 510(k)

TURBO-JET MODEL 76

K-Number: K771969 · 1977-11-02

ApplicantDazey Products Co.
Decision Date1977-11-02
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TURBO-JET MODEL 76 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 1977-11-02 under 510(k) number K771969. 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 TURBO-JET MODEL 76?

TURBO-JET MODEL 76 is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Dazey Products Co.. The 510(k) number is K771969.

When did TURBO-JET MODEL 76 receive FDA 510(k) clearance?

TURBO-JET MODEL 76 received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771969.

Who is the listed applicant for TURBO-JET MODEL 76?

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 TURBO-JET MODEL 76?

The FDA product code for TURBO-JET MODEL 76 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dazey Products Co. as applicant

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.

K771970WHIRLPOOL BATH MODEL 50K771966VIBRO BATH MODEL FS-1K771968WHIRLPOOL BATH MODEL 2273K771967WHIRLPOOL BATH MODEL 2270K771971HYDROMASSAGE EQUIP. MODEL 1000

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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