510(k) K896885

DISPOSABLE RESPIRTORY KIT (MP-200) by Medipart Jerry Alexander — Product Code IYT

K896885 is an FDA 510(k) premarket notification submitted by Medipart Jerry Alexander for the device "DISPOSABLE RESPIRTORY KIT (MP-200)". The FDA issued a decision of Substantially Equivalent on February 26, 1990. The device falls under product code IYT (System, Rebreathing, Radionuclide), a Class II device regulated under 21 CFR 892.1390. Medipart Jerry Alexander has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1990
Date Received
December 8, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Rebreathing, Radionuclide
Device Class
Class II
Regulation Number
892.1390
Review Panel
RA
Submission Type