Field Medical Oxygen Gen/Dist Sys-Battlefield Purp

FDA 510(k) K903411 · Guild Assoc., Inc.

Substantially Equivalent

510(k) numberK903411

Submission

Device name
Field Medical Oxygen Gen/Dist Sys-Battlefield Purp
Applicant
Guild Assoc., Inc.
Hilliard, OH, US
Received
July 30, 1990
Decision date
August 31, 1990
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

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Questions and answers

When was Field Medical Oxygen Gen/Dist Sys-Battlefield Purp cleared by the FDA?

Field Medical Oxygen Gen/Dist Sys-Battlefield Purp (K903411) received a 510(k) decision of Substantially Equivalent on August 31, 1990, 32 days after the submission was received.

What is the product code of K903411?

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