510(k) K864147

AQUAVALVE by Respiratory Care, Inc. — Product Code BYH

K864147 is an FDA 510(k) premarket notification submitted by Respiratory Care, Inc. for the device "AQUAVALVE". The FDA issued a decision of Substantially Equivalent on December 5, 1986. The device falls under product code BYH (Drain, Tee (Water Trap)), a Class I device regulated under 21 CFR 868.5995. Respiratory Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 1986
Date Received
October 22, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drain, Tee (Water Trap)
Device Class
Class I
Regulation Number
868.5995
Review Panel
AN
Submission Type