510(k) K973770

ALLEGIANCE KWIK HEAT WARM PERINEAL PACK by Allegiance Healthcare Corp. — Product Code IMD

K973770 is an FDA 510(k) premarket notification submitted by Allegiance Healthcare Corp. for the device "ALLEGIANCE KWIK HEAT WARM PERINEAL PACK". The FDA issued a decision of Substantially Equivalent on November 13, 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
November 13, 1997
Date Received
October 2, 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