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FDA 510(k)

CRYSTAR(TM) ANTI-GREENING LIQUID

K-Number: K893481 · 1989-07-14

Decision Date1989-07-14
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CRYSTAR(TM) ANTI-GREENING LIQUID is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893481. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYSTAR(TM) ANTI-GREENING LIQUID?

CRYSTAR(TM) ANTI-GREENING LIQUID is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Shofu Dental Corp.. The 510(k) number is K893481.

When did CRYSTAR(TM) ANTI-GREENING LIQUID receive FDA 510(k) clearance?

CRYSTAR(TM) ANTI-GREENING LIQUID received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893481.

Who is the listed applicant for CRYSTAR(TM) ANTI-GREENING LIQUID?

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

What is the FDA product code for CRYSTAR(TM) ANTI-GREENING LIQUID?

The FDA product code for CRYSTAR(TM) ANTI-GREENING LIQUID is ELL.

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 Shofu Dental 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.

View all 59 devices →

Related Devices (Code: ELL)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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