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FDA 510(k)

VOLUREX TM

K-Number: K791015 · 1979-06-13

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1979-06-13
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VOLUREX TM is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. It received FDA 510(k) clearance on 1979-06-13 under 510(k) number K791015. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLUREX TM?

VOLUREX TM is a medical device that received FDA 510(k) clearance on 1979-06-13. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K791015.

When did VOLUREX TM receive FDA 510(k) clearance?

VOLUREX TM received FDA 510(k) clearance on 1979-06-13, under 510(k) number K791015.

Who is the listed applicant for VOLUREX TM?

The FDA 510(k) record lists Dhd Medical Products Div. Diemolding Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOLUREX TM?

The FDA product code for VOLUREX TM is BWF.

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Other records listing Dhd Medical Products Div. Diemolding Corp. as applicant

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Related Devices (Code: BWF)

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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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