510(k) K780011

CONCHAPAK OXYGEN DILUTER by Respiratory Care, Inc. — Product Code BYF

K780011 is an FDA 510(k) premarket notification submitted by Respiratory Care, Inc. for the device "CONCHAPAK OXYGEN DILUTER". The FDA issued a decision of Substantially Equivalent on February 2, 1978. The device falls under product code BYF (Mask, Oxygen, Low Concentration, Venturi), a Class I device regulated under 21 CFR 868.5600. Respiratory Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1978
Date Received
January 3, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mask, Oxygen, Low Concentration, Venturi
Device Class
Class I
Regulation Number
868.5600
Review Panel
AN
Submission Type