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FDA 510(k)

TELESONIC BODY STIMULATOR

K-Number: K872606 · 1987-12-22

ApplicantTelesonic, Inc.
Decision Date1987-12-22
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TELESONIC BODY STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Telesonic, Inc.. It received FDA 510(k) clearance on 1987-12-22 under 510(k) number K872606. 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 TELESONIC BODY STIMULATOR?

TELESONIC BODY STIMULATOR is a medical device that received FDA 510(k) clearance on 1987-12-22. The listed applicant is Telesonic, Inc.. The 510(k) number is K872606.

When did TELESONIC BODY STIMULATOR receive FDA 510(k) clearance?

TELESONIC BODY STIMULATOR received FDA 510(k) clearance on 1987-12-22, under 510(k) number K872606.

Who is the listed applicant for TELESONIC BODY STIMULATOR?

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

What is the FDA product code for TELESONIC BODY STIMULATOR?

The FDA product code for TELESONIC BODY STIMULATOR is IPF.

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Other records listing Telesonic, Inc. 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.

K813329POST-AURICULAR HEARING AID MODEL P-101K813330POST-AURICULAR HEARING AID MODEL S-101K813344POST-AURICULAR HEARING AID MODEL ASP-103K813316CUSTOM-IN-THE-EAR HEARING AIDK811031TELESONIC & ARCONK802596TELESONIC, ARCON & SOUNDEX ASP 102

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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

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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