'TENSAID'— 510(k) K863567

Substantially Equivalent

Electro Therapeutic Devices, Inc.

FDA 510(k) clearance K863567 for 'TENSAID', Substantially Equivalent on 1986-10-24. Applicant: Electro Therapeutic Devices, Inc.. Device class: 2.

Clearance details

Applicant: Electro Therapeutic Devices, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1986-09-12
Decision date: 1986-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Markham, Ontario, CA

Download summary PDF View on FDA.gov ↗

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More clearances from Electro Therapeutic Devices, Inc.

K981272 — ADDIQUIP DISPOSABLE ACUPUNCTURE NEEDLES1998-08-24
K875317 — ELECTRICAL MUSCLE STIMULATOR MODEL MYOAID1989-09-08
K863568 — 'MYOSTIM EX'1986-10-24
K853718 — TRANSCUTANEOUS ELECTR. NERVE STIMUL MYOSTIM 8041985-12-04
K853719 — TRANSCUTANEOUS ELECT. NERVE STIMUL-MYOSTIM 4101985-12-04

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