Model Ipd Oxygen Conserving Device

FDA 510(k) K953852 · Invacare Corp.

Substantially Equivalent

510(k) numberK953852

Submission

Device name
Model Ipd Oxygen Conserving Device
Applicant
Invacare Corp.
Elyria, OH, US
Received
August 16, 1995
Decision date
November 22, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
NFB – Conserver, Oxygen
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5905
Specialty
Anesthesiology

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Questions and answers

When was Model Ipd Oxygen Conserving Device cleared by the FDA?

Model Ipd Oxygen Conserving Device (K953852) received a 510(k) decision of Substantially Equivalent on November 22, 1995, 98 days after the submission was received.

What is the product code of K953852?

The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.