K-number	K850601
Device name	MODEL 1712 CATHETER WITHDRAWAL SYS FOR URETHRAL PR
Applicant	Life-Tech Intl., Inc.
Product code	FAP
Device class	Class II
Decision date	Apr 25, 1985
Decision	Substantially Equivalent
Regulation	876.1620

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View the full FDA submission: accessdata.fda.gov

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MODEL 1712 CATHETER WITHDRAWAL SYS FOR URETHRAL PR

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