19091-XXXXX SER. OF GLASS CAPILLARY COL. (K791893) — FDA 510(k) Clearance | Predicase

K-number	K791893
Device name	19091-XXXXX SER. OF GLASS CAPILLARY COL.
Applicant	Hewlett-Packard Co.
Product code	DII
Device class	Class I
Decision date	Oct 30, 1979
Decision	Substantially Equivalent
Regulation	862.2250

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View the full FDA submission: accessdata.fda.gov

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