REXTON RX12 POWER PLUS W/DUAL RECEIVER— 510(k) K901341

Substantially Equivalent

Rexton, Inc.

FDA 510(k) clearance K901341 for REXTON RX12 POWER PLUS W/DUAL RECEIVER, Substantially Equivalent on 1990-07-27. Applicant: Rexton, Inc..

Clearance details

Applicant: Rexton, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1990-03-22
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plymouth, MN, US

Download summary PDF View on FDA.gov ↗

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