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FDA 510(k)

HEALTH POINT

K-Number: K781651 · 1979-04-03

ApplicantAnritsu America Co.
Decision Date1979-04-03
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

HEALTH POINT is the device name listed in this FDA 510(k) record. The listed applicant is Anritsu America Co.. It received FDA 510(k) clearance on 1979-04-03 under 510(k) number K781651. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEALTH POINT?

HEALTH POINT is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Anritsu America Co.. The 510(k) number is K781651.

When did HEALTH POINT receive FDA 510(k) clearance?

HEALTH POINT received FDA 510(k) clearance on 1979-04-03, under 510(k) number K781651.

Who is the listed applicant for HEALTH POINT?

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

What is the FDA product code for HEALTH POINT?

The FDA product code for HEALTH POINT is BWK.

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.

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Other records listing Anritsu America 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.

K811499TENSMAX

Related Devices (Code: BWK)

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.

K244030Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)Wuxi Jiajian Medical Instrument Co., Ltd.K220153Needle Stimulator (Model: RJNS6-1)Bozhou Rongjian Medical Appliance Co., Ltd.K202861Needle StimulatorWuxi Jiajian Medical Instrument Co., Ltd.K200636AXUS ES-5 Electro-Acupuncture DeviceLhasa Oms, Inc.K170391ANSiStim-PPDyansys, Inc.K152571StivaxBiegler GmbH

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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