Mobin-Vddin Vein Graft Holder
FDA 510(k) K854913 · Pilling Co.
510(k) numberK854913
Submission
- Device name
- Mobin-Vddin Vein Graft Holder
- 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 Mobin-Vddin Vein Graft Holder cleared by the FDA?
Mobin-Vddin Vein Graft Holder (K854913) received a 510(k) decision of Substantially Equivalent on January 24, 1986, 46 days after the submission was received.