Multi-Ported Face Plate
FDA 510(k) K760654 · Pilling Co.
510(k) numberK760654
Submission
- Device name
- Multi-Ported Face Plate
- Applicant
- Pilling Co.
Mchenry, IL, US - Received
- September 16, 1976
- Decision date
- December 6, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Multi-Ported Face Plate cleared by the FDA?
Multi-Ported Face Plate (K760654) received a 510(k) decision of Substantially Equivalent on December 6, 1976, 81 days after the submission was received.