ELECTROSTIM I.F.— 510(k) K873566

Substantially Equivalent

Promatek Industries, Ltd.

FDA 510(k) clearance K873566 for ELECTROSTIM I.F., Substantially Equivalent on 1988-02-01. Applicant: Promatek Industries, Ltd.. Device class: 2.

Clearance details

Applicant: Promatek Industries, Ltd.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1987-09-02
Decision date: 1988-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Quebec, H4p 2c9, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code LIH

K231575 — Vecttor VT-3002024-02-08
K202725 — ETD40002021-03-26
K183692 — Avid IF22019-06-12
K122944 — GEMORE TRUE SINE INTERFERENTIAL STIMULATOR2012-12-21
K121662 — VECTTOR VT-2002012-11-21

More clearances from Promatek Industries, Ltd.

K901417 — ELECTROSTIM MST1990-08-28
K871472 — KINESTIM MUSCLE STIMULATOR1987-06-29

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