DEVO/MC29 Oxygen Concentrator MC29D

FDA 510(k) K852209 · The Devilbiss Co.

Substantially Equivalent

510(k) numberK852209

Submission

Device name
DEVO/MC29 Oxygen Concentrator MC29D
Applicant
The Devilbiss Co.
Somerset, PA, US
Received
May 21, 1985
Decision date
June 24, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

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More from Devilbiss Healthcare, LLC

510(k)DeviceDecision
K874041Devilbiss Model 8500DCAF · Traditional 12/23/1987SE
K872094Vacu-AideJCX · Traditional 10/15/1987SE
K872826Ultra-Neb 99 Ultrasonic NebulizerCAF · Traditional 09/04/1987SE
K872470DEVO/MC44 Oxygen ConcentratorCAW · Traditional 08/03/1987SE
K854520Pulmo-Aide Model 5610DCCQ · Traditional 12/09/1985SE
K851695Ultra-Neb 100 Ultrasonic Nebulizer · Traditional 06/05/1985SE
K830174De VO/44 Oxygen Concentrator #444CAW · Traditional 02/17/1983SE
K801526Surveyor I, Respiratory Computer SystemBZC · Traditional 07/21/1980SE
K792385Devo Oxygen Concentrator, Model 955CAW · Traditional 12/05/1979SE
K781073Pulmo-SonicCCQ · Traditional 09/27/1978SE

Questions and answers

When was DEVO/MC29 Oxygen Concentrator MC29D cleared by the FDA?

DEVO/MC29 Oxygen Concentrator MC29D (K852209) received a 510(k) decision of Substantially Equivalent on June 24, 1985, 34 days after the submission was received.

What is the product code of K852209?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.