Pagewriter 200, 200I Cardiograph & Interpretive Cardio
FDA 510(k) K954980 · Hewlett-Packard Co.
510(k) numberK954980
Submission
- Device name
- Pagewriter 200, 200I Cardiograph & Interpretive Cardio
- Applicant
- Hewlett-Packard Co.
Mcminnville, OR, US - Received
- October 31, 1995
- Decision date
- May 15, 1996
- 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 200, 200I Cardiograph & Interpretive Cardio cleared by the FDA?
Pagewriter 200, 200I Cardiograph & Interpretive Cardio (K954980) received a 510(k) decision of Substantially Equivalent on May 15, 1996, 197 days after the submission was received.