INOBLENDER— 510(k) K122689

Substantially Equivalent

Ino Therapeutics

FDA 510(k) clearance K122689 for INOBLENDER, Substantially Equivalent on 2012-11-07. Applicant: Ino Therapeutics. Device class: 2.

Clearance details

Applicant: Ino Therapeutics
Product code: Code MRO
Device class: Class 2
Regulation: 21 CFR 868.5165
Advisory panel: Anesthesiology
Date received: 2012-09-04
Decision date: 2012-11-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Madison, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MRO

K052663 — INO THERAPEUTICS INOBLENDER, MODEL 100042005-11-04
K011874 — FADASIS MEDICAL FM-1 NO BLENDER2001-07-20
K003665 — FADASSI MEDICAL FM-1 NO BLENDER2001-02-23

More clearances from Ino Therapeutics

K130605 — INOMAX DSIR (DELIVERY SYSTEM)2013-05-02
K121021 — INOMAX DS (DELIVERY SYSTEM)2012-09-24
K110344 — INOMAX DSIR (DELIVERY SYSTEM)2011-06-24
K093922 — INOMAX DS2010-04-15
K080484 — INOMAX DS (DELIVERY SYSTEM), MODEL 100032008-08-06

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