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FDA 510(k)

PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF

K-Number: K913931 · 1992-03-04

ApplicantAbbott Laboratories
Decision Date1992-03-04
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1992-03-04 under 510(k) number K913931. 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 PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF?

PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Abbott Laboratories. The 510(k) number is K913931.

When did PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF receive FDA 510(k) clearance?

PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF received FDA 510(k) clearance on 1992-03-04, under 510(k) number K913931.

Who is the listed applicant for PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF?

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 PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF?

The FDA product code for PANCRETEC PROVIDER(R) MODEL 5500 INFUS PUMP, MODIF is 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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