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FDA 510(k)

522 INTELLIGENT PUMP

K-Number: K882159 · 1988-08-24

ApplicantKendall Mcgaw Laboratories, Inc.
Decision Date1988-08-24
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

522 INTELLIGENT PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Mcgaw Laboratories, Inc.. It received FDA 510(k) clearance on 1988-08-24 under 510(k) number K882159. 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 522 INTELLIGENT PUMP?

522 INTELLIGENT PUMP is a medical device that received FDA 510(k) clearance on 1988-08-24. The listed applicant is Kendall Mcgaw Laboratories, Inc.. The 510(k) number is K882159.

When did 522 INTELLIGENT PUMP receive FDA 510(k) clearance?

522 INTELLIGENT PUMP received FDA 510(k) clearance on 1988-08-24, under 510(k) number K882159.

Who is the listed applicant for 522 INTELLIGENT PUMP?

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

What is the FDA product code for 522 INTELLIGENT PUMP?

The FDA product code for 522 INTELLIGENT PUMP is FRN.

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Other records listing Kendall Mcgaw Laboratories, Inc. as applicant

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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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