K863007Substantially Equivalent

Euroflex F-IV, Isoflex III

Name: K863007 Euroflex F-IV, Isoflex III
Creator: Sds Dental, Inc.
Published: 1986-10-01
License: https://open.fda.gov/license/

Sds Dental, Inc., Washington DC / Traditional, Substantially Equivalent

FDA source

K863007 is the FDA 510(k) clearance record for EUROFLEX F-IV, ISOFLEX III, cleared for Sds Dental, Inc. on 1986-10-01. FDA records list 21 510(k) clearances for Sds Dental, Inc., from 1986-09-24 to 1999-11-05. As of 2026-09-10, FDA records show no recalls naming K863007.

Clearance record

Decision date: 1986-10-01
Received: 1986-08-08 (54 days to decision)
Review panel: Unknown
Applicant: Sds Dental, Inc. 4321 Wisconsin Ave. N.W, Washington DC
Third party review: No