510(k) K872037

AEROCHAMBER by Monaghan Medical Corp. — Product Code BYP

K872037 is an FDA 510(k) premarket notification submitted by Monaghan Medical Corp. for the device "AEROCHAMBER". The FDA issued a decision of Substantially Equivalent on July 24, 1987. The device falls under product code BYP (Mouthpiece, Breathing), a Class I device regulated under 21 CFR 868.5620. Monaghan Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 24, 1987
Date Received
May 27, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mouthpiece, Breathing
Device Class
Class I
Regulation Number
868.5620
Review Panel
AN
Submission Type