K-number	K913136
Device name	LASER ENDOSCOPE DISC DECOMPRESSION KITS
Applicant	Medical Laser, Inc.
Product code	LRO
Device class	Class II
Decision date	Nov 1, 1991
Decision	Unknown
Regulation	878.4370

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Source

View the full FDA submission: accessdata.fda.gov

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LASER ENDOSCOPE DISC DECOMPRESSION KITS

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