510(k) K811711

PEDIATRIC OXYGEN MASKS by Airlife, Inc. — Product Code BYG

K811711 is an FDA 510(k) premarket notification submitted by Airlife, Inc. for the device "PEDIATRIC OXYGEN MASKS". The FDA issued a decision of Substantially Equivalent on July 1, 1981. The device falls under product code BYG (Mask, Oxygen), a Class I device regulated under 21 CFR 868.5580. Airlife, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 1, 1981
Date Received
June 17, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mask, Oxygen
Device Class
Class I
Regulation Number
868.5580
Review Panel
AN
Submission Type