K-number	K822328
Device name	IL 301 TRANSCUTANEOUS OXYGEN MONITOR
Applicant	Instrumentation Laboratory CO
Product code	KLK
Device class	Class II
Decision date	Sep 7, 1982
Decision	Substantially Equivalent
Regulation	868.2500

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View the full FDA submission: accessdata.fda.gov

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IL 301 TRANSCUTANEOUS OXYGEN MONITOR

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