K-number	K790009
Device name	ICE PACK, REUSABLE FLEXIBLE
Applicant	Ackrad Laboratories
Product code	IME
Device class	Class I
Decision date	Jan 22, 1979
Decision	Substantially Equivalent
Regulation	890.5700

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View the full FDA submission: accessdata.fda.gov

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ICE PACK, REUSABLE FLEXIBLE

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