Pagewriter 200I Interpretive Cardiograph Model M1770A with Acute Cardiac Ischemia Time Insensitive Predictive Instrumena
FDA 510(k) K981265 · Hewlett-Packard Co.
510(k) numberK981265
Submission
- Device name
- Pagewriter 200I Interpretive Cardiograph Model M1770A with Acute Cardiac Ischemia Time Insensitive Predictive Instrumena
- Applicant
- Hewlett-Packard Co.
North Attleboro, MA, US - Received
- April 7, 1998
- Decision date
- June 23, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
No product code recorded.
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Questions and answers
When was Pagewriter 200I Interpretive Cardiograph Model M1770A with Acute Cardiac Ischemia Time Insensitive Predictive Instrumena cleared by the FDA?
Pagewriter 200I Interpretive Cardiograph Model M1770A with Acute Cardiac Ischemia Time Insensitive Predictive Instrumena (K981265) received a 510(k) decision of Substantially Equivalent on June 23, 1998, 77 days after the submission was received.