510(k) K970399

KWIK KOLD PERI COLD PACK (CATALOG NUMBER TBD) by Allegiance Healthcare Corp. — Product Code IMD

K970399 is an FDA 510(k) premarket notification submitted by Allegiance Healthcare Corp. for the device "KWIK KOLD PERI COLD PACK (CATALOG NUMBER TBD)". The FDA issued a decision of Substantially Equivalent on April 3, 1997. The device falls under product code IMD (Pack, Hot Or Cold, Disposable), a Class I device regulated under 21 CFR 890.5710. Allegiance Healthcare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 3, 1997
Date Received
February 3, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pack, Hot Or Cold, Disposable
Device Class
Class I
Regulation Number
890.5710
Review Panel
PM
Submission Type