TELESONIC BODY STIMULATOR— 510(k) K872606

Substantially Equivalent

Telesonic, Inc.

FDA 510(k) clearance K872606 for TELESONIC BODY STIMULATOR, Substantially Equivalent on 1987-12-22. Applicant: Telesonic, Inc.. Device class: 2.

Clearance details

Applicant: Telesonic, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1987-07-02
Decision date: 1987-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Telesonic, Inc.

K813329 — POST-AURICULAR HEARING AID MODEL P-1011982-01-19
K813330 — POST-AURICULAR HEARING AID MODEL S-1011982-01-19
K813316 — CUSTOM-IN-THE-EAR HEARING AID1981-12-31
K813344 — POST-AURICULAR HEARING AID MODEL ASP-1031981-12-31
K811031 — TELESONIC & ARCON1981-07-01

Data sourced from openFDA. This site is unofficial and independent of the FDA.