DISPOS. PRESSURE KIT 1295K SERIES

Transducer, Blood-pressure, Extravascular

HEWLETT-PACKARD CO.

The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Dispos. Pressure Kit 1295k Series.

Pre-market Notification Details

Device IDK843273
510k NumberK843273
Device Name:DISPOS. PRESSURE KIT 1295K SERIES
ClassificationTransducer, Blood-pressure, Extravascular
Applicant HEWLETT-PACKARD CO. 4221 Richmond Rd., N.W. Walker,  MI  49534
Product CodeDRS  
CFR Regulation Number870.2850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-08-20
Decision Date1985-06-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.