510(k) K842050

IMPACT MODEL 316 by Impact Instrumentation, Inc. — Product Code JCX

K842050 is an FDA 510(k) premarket notification submitted by Impact Instrumentation, Inc. for the device "IMPACT MODEL 316". The FDA issued a decision of Substantially Equivalent on August 3, 1984. 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
August 3, 1984
Date Received
May 22, 1984
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