CMT 1000— 510(k) K852390

Substantially Equivalent

Prestigeline, Inc.

FDA 510(k) clearance K852390 for CMT 1000, Substantially Equivalent on 1985-07-19. Applicant: Prestigeline, Inc.. Device class: 1.

Clearance details

Applicant: Prestigeline, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1985-06-05
Decision date: 1985-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brentwood, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQX

K011827 — ORTELIUS 8002001-08-28
K971079 — INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE1997-07-09
K962377 — 3D-SPINE1996-09-03
K961212 — SPINAL TOUCH1996-06-12
K954647 — INCLINOMETER1995-10-30

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