DURA-PATCH MODEL DP-XXX (K980548) — FDA 510(k) Clearance | Predicase

K-number	K980548
Device name	DURA-PATCH MODEL DP-XXX
Applicant	Bridger Biomed, Inc.
Product code	GXQ
Device class	Class II
Decision date	May 13, 1998
Decision	Substantially Equivalent
Regulation	882.5910

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View the full FDA submission: accessdata.fda.gov

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