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FDA 510(k)

VOFLEX

K-Number: K840239 · 1984-03-05

ApplicantDhd Medical Products Div. Diemolding Corp.
Decision Date1984-03-05
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VOFLEX 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 1984-03-05 under 510(k) number K840239. 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 VOFLEX?

VOFLEX is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Dhd Medical Products Div. Diemolding Corp.. The 510(k) number is K840239.

When did VOFLEX receive FDA 510(k) clearance?

VOFLEX received FDA 510(k) clearance on 1984-03-05, under 510(k) number K840239.

Who is the listed applicant for VOFLEX?

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 VOFLEX?

The FDA product code for VOFLEX 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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