510(k) K133196

IMPACT MODEL 323 ASPIRATOR by Impact Instrumentation, Inc. — Product Code JCX

K133196 is an FDA 510(k) premarket notification submitted by Impact Instrumentation, Inc. for the device "IMPACT MODEL 323 ASPIRATOR". The FDA issued a decision of Substantially Equivalent on March 10, 2014. The device falls under product code JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered), a Class II device regulated under 21 CFR 878.4780. Impact Instrumentation, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 2014
Date Received
October 17, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device Class
Class II
Regulation Number
878.4780
Review Panel
SU
Submission Type