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FDA 510(k)

AUTO SYRINGE AS40A INFUSION PUMP

K-Number: K940147 · 1994-04-15

ApplicantBaxter Corp.
Decision Date1994-04-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTO SYRINGE AS40A INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Corp.. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K940147. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SYRINGE AS40A INFUSION PUMP?

AUTO SYRINGE AS40A INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Baxter Corp.. The 510(k) number is K940147.

When did AUTO SYRINGE AS40A INFUSION PUMP receive FDA 510(k) clearance?

AUTO SYRINGE AS40A INFUSION PUMP received FDA 510(k) clearance on 1994-04-15, under 510(k) number K940147.

Who is the listed applicant for AUTO SYRINGE AS40A INFUSION PUMP?

The FDA 510(k) record lists Baxter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO SYRINGE AS40A INFUSION PUMP?

The FDA product code for AUTO SYRINGE AS40A INFUSION PUMP is FRN.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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