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FDA 510(k)

DISPOSABLE PROPHY ANGLE AND ACCESSORIES

K-Number: K897101 · 1990-03-14

Decision Date1990-03-14
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PROPHY ANGLE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1990-03-14 under 510(k) number K897101. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE PROPHY ANGLE AND ACCESSORIES?

DISPOSABLE PROPHY ANGLE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1990-03-14. The listed applicant is Dentsply Intl.. The 510(k) number is K897101.

When did DISPOSABLE PROPHY ANGLE AND ACCESSORIES receive FDA 510(k) clearance?

DISPOSABLE PROPHY ANGLE AND ACCESSORIES received FDA 510(k) clearance on 1990-03-14, under 510(k) number K897101.

Who is the listed applicant for DISPOSABLE PROPHY ANGLE AND ACCESSORIES?

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

What is the FDA product code for DISPOSABLE PROPHY ANGLE AND ACCESSORIES?

The FDA product code for DISPOSABLE PROPHY ANGLE AND ACCESSORIES is EFB.

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 Dentsply Intl. 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 279 devices →

Related Devices (Code: EFB)

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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