K-number	K770410
Device name	BANDAGE COMPRESS 2, 3, 4
Applicant	Johnson & Johnson Professionals, Inc.
Product code	NAB
Device class	Class I
Decision date	Jun 9, 1977
Decision	Substantially Equivalent
Regulation	878.4014

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View the full FDA submission: accessdata.fda.gov

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BANDAGE COMPRESS 2, 3, 4

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