FZH — Apparatus, Air Handling, Room Class II

FDA Device Classification

FDA product code FZH covers "Apparatus, Air Handling, Room", a Class II medical device regulated under 21 CFR 878.5070. Submissions are reviewed by the General, Plastic Surgery panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
FZH
Device Class
Class II
Regulation Number
878.5070
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K923233cardio-med-associatesCARDIO-PAK LAPAROTOMY PACKMarch 20, 1993
K875305spec systemsMODEL UCA / SPEC SYSTEM UCAJanuary 27, 1988
K871901custom industriesULTRAFLOWJune 1, 1987
K770084dupacoOPERATING ROOM VENTILATORFebruary 23, 1977