510(k) K831795

FIRST AID KITS by I M, Inc. — Product Code KDD

K831795 is an FDA 510(k) premarket notification submitted by I M, Inc. for the device "FIRST AID KITS". The FDA issued a decision of Substantially Equivalent on September 1, 1983. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. I M, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 1, 1983
Date Received
June 3, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Surgical Instrument, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type