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FDA 510(k)

MINIFUGE, MODEL 70

K-Number: K882149 · 1988-07-01

ApplicantUtah Bioresearch, Inc.
Decision Date1988-07-01
Product CodeGPG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINIFUGE, MODEL 70 is the device name listed in this FDA 510(k) record. The listed applicant is Utah Bioresearch, Inc.. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K882149. The device is classified under product code GPG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIFUGE, MODEL 70?

MINIFUGE, MODEL 70 is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is Utah Bioresearch, Inc.. The 510(k) number is K882149.

When did MINIFUGE, MODEL 70 receive FDA 510(k) clearance?

MINIFUGE, MODEL 70 received FDA 510(k) clearance on 1988-07-01, under 510(k) number K882149.

Who is the listed applicant for MINIFUGE, MODEL 70?

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

What is the FDA product code for MINIFUGE, MODEL 70?

The FDA product code for MINIFUGE, MODEL 70 is GPG.

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Related Devices (Code: GPG)

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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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