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FDA 510(k)

DHD EMERALD PRODUCT

K-Number: K970596 · 1997-05-16

ApplicantDhd Diemolding Healthcare Div.
Decision Date1997-05-16
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DHD EMERALD PRODUCT is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Diemolding Healthcare Div.. It received FDA 510(k) clearance on 1997-05-16 under 510(k) number K970596. 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 DHD EMERALD PRODUCT?

DHD EMERALD PRODUCT is a medical device that received FDA 510(k) clearance on 1997-05-16. The listed applicant is Dhd Diemolding Healthcare Div.. The 510(k) number is K970596.

When did DHD EMERALD PRODUCT receive FDA 510(k) clearance?

DHD EMERALD PRODUCT received FDA 510(k) clearance on 1997-05-16, under 510(k) number K970596.

Who is the listed applicant for DHD EMERALD PRODUCT?

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

What is the FDA product code for DHD EMERALD PRODUCT?

The FDA product code for DHD EMERALD PRODUCT is 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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