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FDA 510(k)

M.I.P. - PUMP

K-Number: K882249 · 1989-02-28

ApplicantIntro-Med, Inc.
Decision Date1989-02-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

M.I.P. - PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Intro-Med, Inc.. It received FDA 510(k) clearance on 1989-02-28 under 510(k) number K882249. 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 M.I.P. - PUMP?

M.I.P. - PUMP is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Intro-Med, Inc.. The 510(k) number is K882249.

When did M.I.P. - PUMP receive FDA 510(k) clearance?

M.I.P. - PUMP received FDA 510(k) clearance on 1989-02-28, under 510(k) number K882249.

Who is the listed applicant for M.I.P. - PUMP?

The FDA 510(k) record lists Intro-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M.I.P. - PUMP?

The FDA product code for M.I.P. - PUMP is FRN.

Related Devices (Code: FRN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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