Pilling Disposable Aorta Punch
FDA 510(k) K854915 · Pilling Co.
510(k) numberK854915
Submission
- Device name
- Pilling Disposable Aorta Punch
- Applicant
- Pilling Co.
Fort Washington, PA, US - Received
- December 9, 1985
- Decision date
- January 24, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Pilling Disposable Aorta Punch cleared by the FDA?
Pilling Disposable Aorta Punch (K854915) received a 510(k) decision of Substantially Equivalent on January 24, 1986, 46 days after the submission was received.