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FDA 510(k)

3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION)

K-Number: K940446 · 1994-08-15

ApplicantMinnesota Mining and Mfg. Co.
Decision Date1994-08-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Mining and Mfg. Co.. It received FDA 510(k) clearance on 1994-08-15 under 510(k) number K940446. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION)?

3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1994-08-15. The listed applicant is Minnesota Mining and Mfg. Co.. The 510(k) number is K940446.

When did 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) receive FDA 510(k) clearance?

3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) received FDA 510(k) clearance on 1994-08-15, under 510(k) number K940446.

Who is the listed applicant for 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION)?

The FDA 510(k) record lists Minnesota Mining and Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION)?

The FDA product code for 3M MODEL 3000 & MODEL 3100 INFUSION PUMP (MODIFICATION) is FRN.

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Related Devices (Code: FRN)

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Official Source

View on FDA Database →

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

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