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FDA 510(k), K861276, TAMPER PROOF CAP
FDA 510(k), K861276, TAMPER PROOF CAP
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510(K) Number: K861276
Device Name: TAMPER PROOF CAP
Manufacturer: JOHN P VITELLO
Device Classification Name: Syringe, Piston
Regulation Number: FMF
Classification Product Code: KXA
Date Received: 04/07/1986
Decision Date: 05/05/1986
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: TAMPER PROOF CAP
Manufacturer: JOHN P VITELLO
Device Classification Name: Syringe, Piston
Regulation Number: FMF
Classification Product Code: KXA
Date Received: 04/07/1986
Decision Date: 05/05/1986
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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