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FDA 510(k)

DURALIFE(TM)

K-Number: K913726 · 1992-02-07

ApplicantDhd Diemolding Healthcare Div.
Decision Date1992-02-07
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DURALIFE(TM) 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 1992-02-07 under 510(k) number K913726. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURALIFE(TM)?

DURALIFE(TM) is a medical device that received FDA 510(k) clearance on 1992-02-07. The listed applicant is Dhd Diemolding Healthcare Div.. The 510(k) number is K913726.

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

DURALIFE(TM) received FDA 510(k) clearance on 1992-02-07, under 510(k) number K913726.

Who is the listed applicant for DURALIFE(TM)?

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 DURALIFE(TM)?

The FDA product code for DURALIFE(TM) is BZA.

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Other records listing Dhd Diemolding Healthcare Div. as applicant

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Related Devices (Code: BZA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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