K-number	K122905
Device name	PEREGRINE 23GA CURVED LASER PROBE
Applicant	Peregrine Surgical , Ltd.
Product code	HQB
Device class	Class II
Decision date	Apr 30, 2013
Decision	Substantially Equivalent
Regulation	886.4690

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Source

View the full FDA submission: accessdata.fda.gov

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PEREGRINE 23GA CURVED LASER PROBE

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