PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO

510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products   510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la

HEWLETT-PACKARD CO.

The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Pagewriter 200, 200i Cardiograph & Interpretive Cardio.

Pre-market Notification Details

Device IDK954980
510k NumberK954980
Device Name:PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO
Classification510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products   510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la
Applicant HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville,  OR  97128
ContactNancy Winn
CorrespondentNancy Winn
HEWLETT-PACKARD CO. 1700 SOUTH BAKER ST. Mcminnville,  OR  97128
Product CodeLOS
CFR Regulation Number510(k) Premarket Notification [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-10-31
Decision Date1996-05-15
Summary:summary

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