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FDA 510(k)

HIGH SILVER CONVENTIONAL

K-Number: K020452 · 2002-05-07

ApplicantAb Ardent
Decision Date2002-05-07
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HIGH SILVER CONVENTIONAL is the device name listed in this FDA 510(k) record. The listed applicant is Ab Ardent. It received FDA 510(k) clearance on 2002-05-07 under 510(k) number K020452. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH SILVER CONVENTIONAL?

HIGH SILVER CONVENTIONAL is a medical device that received FDA 510(k) clearance on 2002-05-07. The listed applicant is Ab Ardent. The 510(k) number is K020452.

When did HIGH SILVER CONVENTIONAL receive FDA 510(k) clearance?

HIGH SILVER CONVENTIONAL received FDA 510(k) clearance on 2002-05-07, under 510(k) number K020452.

Who is the listed applicant for HIGH SILVER CONVENTIONAL?

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

What is the FDA product code for HIGH SILVER CONVENTIONAL?

The FDA product code for HIGH SILVER CONVENTIONAL is EJJ.

Related Clinical Trials

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.

Other records listing Ab Ardent as applicant

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.

View all 13 devices →

Related Devices (Code: EJJ)

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.

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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