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FDA 510(k)

HYDROTONE-THERMAL CAPSULE SYSTEM

K-Number: K991184 · 1999-06-23

ApplicantNats Corp.
Decision Date1999-06-23
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HYDROTONE-THERMAL CAPSULE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nats Corp.. It received FDA 510(k) clearance on 1999-06-23 under 510(k) number K991184. 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 HYDROTONE-THERMAL CAPSULE SYSTEM?

HYDROTONE-THERMAL CAPSULE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-23. The listed applicant is Nats Corp.. The 510(k) number is K991184.

When did HYDROTONE-THERMAL CAPSULE SYSTEM receive FDA 510(k) clearance?

HYDROTONE-THERMAL CAPSULE SYSTEM received FDA 510(k) clearance on 1999-06-23, under 510(k) number K991184.

Who is the listed applicant for HYDROTONE-THERMAL CAPSULE SYSTEM?

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

What is the FDA product code for HYDROTONE-THERMAL CAPSULE SYSTEM?

The FDA product code for HYDROTONE-THERMAL CAPSULE SYSTEM is ILJ.

Related Clinical Trials

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Other records listing Nats Corp. 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.

K040143MONORAILK033142POWERED WHEELCHAIRK020060ASTOFLOK011820DENTORIUM CONVERTIBLE ACRYLIC

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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