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FDA 510(k)

UVP VOLUMED 2001

K-Number: K881079 · 1988-10-25

ApplicantFerguson Medical
Decision Date1988-10-25
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UVP VOLUMED 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-10-25 under 510(k) number K881079. 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 UVP VOLUMED 2001?

UVP VOLUMED 2001 is a medical device that received FDA 510(k) clearance on 1988-10-25. The listed applicant is Ferguson Medical. The 510(k) number is K881079.

When did UVP VOLUMED 2001 receive FDA 510(k) clearance?

UVP VOLUMED 2001 received FDA 510(k) clearance on 1988-10-25, under 510(k) number K881079.

Who is the listed applicant for UVP VOLUMED 2001?

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

What is the FDA product code for UVP VOLUMED 2001?

The FDA product code for UVP VOLUMED 2001 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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