K-number	K790958
Device name	120 WELL HISTO-PLATE
Applicant	Dynatech Laboratories, Inc.
Product code	KIZ
Device class	Class I
Decision date	Jun 28, 1979
Decision	Substantially Equivalent
Regulation	864.2240

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View the full FDA submission: accessdata.fda.gov

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120 WELL HISTO-PLATE

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