Model M1792A Thrombolytic Predictive Instrument
FDA 510(k) K974087 · Hewlett-Packard Co.
510(k) numberK974087
Submission
- Device name
- Model M1792A Thrombolytic Predictive Instrument
- Applicant
- Hewlett-Packard Co.
Andover, MA, US - Received
- October 29, 1997
- Decision date
- June 15, 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 Model M1792A Thrombolytic Predictive Instrument cleared by the FDA?
Model M1792A Thrombolytic Predictive Instrument (K974087) received a 510(k) decision of Substantially Equivalent on June 15, 1998, 229 days after the submission was received.