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FDA 510(k)

NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION

K-Number: K910213 · 1991-04-16

ApplicantAbbott Laboratories
Decision Date1991-04-16
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1991-04-16 under 510(k) number K910213. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION?

NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Abbott Laboratories. The 510(k) number is K910213.

When did NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION receive FDA 510(k) clearance?

NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION received FDA 510(k) clearance on 1991-04-16, under 510(k) number K910213.

Who is the listed applicant for NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION?

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

What is the FDA product code for NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION?

The FDA product code for NUTRIMIX(R) MACRO(TM) TPN COMPOUNDER/MODIFICATION is LHI.

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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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