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FDA 510(k)

STABILOR HN

K-Number: K973288 · 1997-11-19

ApplicantDegussa Corp.
Decision Date1997-11-19
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STABILOR HN is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Corp.. It received FDA 510(k) clearance on 1997-11-19 under 510(k) number K973288. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STABILOR HN?

STABILOR HN is a medical device that received FDA 510(k) clearance on 1997-11-19. The listed applicant is Degussa Corp.. The 510(k) number is K973288.

When did STABILOR HN receive FDA 510(k) clearance?

STABILOR HN received FDA 510(k) clearance on 1997-11-19, under 510(k) number K973288.

Who is the listed applicant for STABILOR HN?

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

What is the FDA product code for STABILOR HN?

The FDA product code for STABILOR HN is EJS.

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Other records listing Degussa Corp. 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.

K972910PORS ON LITEK960256DEGUDENT LSK960226DG 88K960104BIOCCLUS 4K955465DEGUPRINTK955118DEGUBOND X-LITE PLUS

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020194SIMIDUR KF PLUSWieland Dental + Technik GmbH & Co. KG

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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