K850872Substantially Equivalent for Some Indications

Phyaction 300, 360, 370, 390 & 391 Elec-Muscle-Sti

Name: K850872 Phyaction 300, 360, 370, 390 & 391 Elec-Muscle-Sti
Creator: Ketronic, Inc.
Published: 1985-06-06
License: https://open.fda.gov/license/

Ketronic, Inc., The Netherlands, NL / Traditional, Substantially Equivalent for Some Indications

FDA source

K850872 is the FDA 510(k) clearance record for PHYACTION 300, 360, 370, 390 & 391 ELEC-MUSCLE-STI, cleared for Ketronic, Inc. on 1985-06-06. FDA records list 10 510(k) clearances for Ketronic, Inc., from 1984-11-08 to 1985-06-12. As of 2026-09-10, FDA records show no recalls naming K850872.

Clearance record

Decision date: 1985-06-06
Received: 1985-03-01 (97 days to decision)
Review panel: Unknown
Applicant: Ketronic, Inc. Duinkerkenlaan 31, The Netherlands, NL
Third party review: No