Quinton Model Q710 Exercise and Resting Electrocardiograph
FDA 510(k) K961014 · Quinton, Inc.
510(k) numberK961014
Submission
- Device name
- Quinton Model Q710 Exercise and Resting Electrocardiograph
- Applicant
- Quinton, Inc.
Bothell, WA, US - Received
- March 13, 1996
- Decision date
- July 31, 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 Quinton Model Q710 Exercise and Resting Electrocardiograph cleared by the FDA?
Quinton Model Q710 Exercise and Resting Electrocardiograph (K961014) received a 510(k) decision of Substantially Equivalent on July 31, 1996, 140 days after the submission was received.