Model 3000 Infusion Pump
FDA 510(k) K871881 · Bd Becton Dickinson Vacutainer Systems Preanalytic
510(k) numberK871881
Submission
- Device name
- Model 3000 Infusion Pump
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US - Received
- May 14, 1987
- Decision date
- January 6, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FRN – Pump, Infusion
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5725
- Specialty
- General Hospital
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| K993186 | Synercid, 15 Ug, BBL Sensi-DiscJTN · Traditional | 11/03/1999SE |
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Questions and answers
When was Model 3000 Infusion Pump cleared by the FDA?
Model 3000 Infusion Pump (K871881) received a 510(k) decision of Substantially Equivalent on January 6, 1988, 237 days after the submission was received.
What is the product code of K871881?
The FDA product code is FRN – Pump, Infusion, a Class II (moderate risk) device regulated under 21 CFR 880.5725.