OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE— 510(k) K973463

Name: FDA 510(k) clearance K973463
Creator: U.S. Food and Drug Administration
Published: 1997-12-02

Substantially Equivalent

O Tech, Inc.

FDA 510(k) clearance K973463 for OLICON IMAGING SYSTEMS, INC. ARCHIVE SYSTEMS, NT ARCHIVE, 02ARCHIVE, ARCHIVE, Substantially Equivalent on 1997-12-02. Applicant: O Tech, Inc.. Device class: 1.

Clearance details

Applicant: O Tech, Inc.
Product code: Code LMB
Device class: Class 1
Regulation: 21 CFR 892.2010
Advisory panel: Radiology
Date received: 1997-09-12
Decision date: 1997-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plano, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMB

view all

K992131 — SAMSUNG RAYPAX LONG TERM ARCHIVE1999-09-13
K984405 — ECHOLIVE FAMILY, MODELS: ZL-1010,ZL-2000,ZL-2100,ZL-3000,ZL-40001999-02-08
K983447 — WISE (II) IMAGE MANAGEMENT SYSTEM1998-10-29
K980243 — PARAMETER DEVELOPMENTS DICOM ARCHIVAL SERVER, (DAS)/DICOM INTRANET SERVICE (DIS)1998-04-03
K973413 — ID. STORE (RELEASE 2.0)1997-11-25

More clearances from O Tech, Inc.

view all

K991643 — IDS4 V3.2 IMAGE DISPLAY SYSTEM1999-06-08
K971368 — IDS4 IMAGE DISPLAY SYSTEM SERIES1997-06-26
K971451 — WISE IMAGE MANAGEMENT SYSTEM1997-06-26

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