OCTOPAQUE UNIVERSAL— 510(k) K942916

Substantially Equivalent

Octostop, Inc.

FDA 510(k) clearance K942916 for OCTOPAQUE UNIVERSAL, Substantially Equivalent on 1994-09-08. Applicant: Octostop, Inc.. Device class: 2.

Clearance details

Applicant: Octostop, Inc.
Product code: Code IXQ
Device class: Class 2
Regulation: 21 CFR 892.1980
Advisory panel: Radiology
Date received: 1994-06-21
Decision date: 1994-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc., CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXQ

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K954225 — MED-TEC HAND GRIP1995-11-14
K946262 — EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLES1995-02-15
K942190 — ID100 MOBILE FLUOROSCOPIC EXAMINING TABLE1994-08-17

More clearances from Octostop, Inc.

K972766 — PIVOTING COMPENSATING FILTERS FOR THE HEAD1997-08-14
K963941 — THE PHARAOH COMPENSATING FILTER1996-11-27
K953246 — OCTOROLL1995-09-29
K952871 — RIDGES PLUS1995-07-20
K940306 — OCTOSTOP COMPENSATING FILTERS1994-09-06

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