510(k) K914283

THAYER EXPANSION CHAMBER METERED DOSE INHALER by Thayer Medical Corp. — Product Code CAF

K914283 is an FDA 510(k) premarket notification submitted by Thayer Medical Corp. for the device "THAYER EXPANSION CHAMBER METERED DOSE INHALER". The FDA issued a decision of Substantially Equivalent on February 26, 1992. The device falls under product code CAF (Nebulizer (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5630. Thayer Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1992
Date Received
September 24, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nebulizer (Direct Patient Interface)
Device Class
Class II
Regulation Number
868.5630
Review Panel
AN
Submission Type