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FDA 510(k)

THER-A-PULSE

K-Number: K872970 · 1987-11-23

ApplicantWestec Corp.
Decision Date1987-11-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THER-A-PULSE is the device name listed in this FDA 510(k) record. The listed applicant is Westec Corp.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K872970. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THER-A-PULSE?

THER-A-PULSE is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Westec Corp.. The 510(k) number is K872970.

When did THER-A-PULSE receive FDA 510(k) clearance?

THER-A-PULSE received FDA 510(k) clearance on 1987-11-23, under 510(k) number K872970.

Who is the listed applicant for THER-A-PULSE?

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

What is the FDA product code for THER-A-PULSE?

The FDA product code for THER-A-PULSE is IPF.

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 Westec 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.

K884396MODIFIED THER-A-PULSE UNIT

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

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