Arterial Graft Sizers
FDA 510(k) K761141 · Pilling Co.
510(k) numberK761141
Submission
- Device name
- Arterial Graft Sizers
- Applicant
- Pilling Co.
Mchenry, IL, US - Received
- November 26, 1976
- Decision date
- January 6, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Arterial Graft Sizers cleared by the FDA?
Arterial Graft Sizers (K761141) received a 510(k) decision of Substantially Equivalent on January 6, 1977, 41 days after the submission was received.