Nebulizer Accessory for Servo Ventill

FDA 510(k) K832898 · Siemens Elema AB

Substantially Equivalent

510(k) numberK832898

Submission

Device name
Nebulizer Accessory for Servo Ventill
Applicant
Siemens Elema AB
Mchenry, IL, US
Received
August 26, 1983
Decision date
November 25, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAF – Nebulizer (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

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More from Aerogen, Ltd.

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K002137Cathcor DesktopDQK · Traditional 10/05/2000SE
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K970839Servo Ventilator 300ACBK · Traditional 10/14/1997ST
K960168Siemens Servo Screen 390 and Servo Computer Module 990CBK · Traditional 10/25/1996ST
K960010Servo Ventilator 300 Computer InterfaceCBK · Traditional 10/25/1996ST
K872278Siemens O2-AIR Mixer 965BZR · Traditional 09/03/1987SE
K871354Servo Ventilator 900 C/DCBK · Traditional 07/21/1987SE

Questions and answers

When was Nebulizer Accessory for Servo Ventill cleared by the FDA?

Nebulizer Accessory for Servo Ventill (K832898) received a 510(k) decision of Substantially Equivalent on November 25, 1983, 91 days after the submission was received.

What is the product code of K832898?

The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.