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FDA 510(k)

AH PLUS ROOT CANAL SEALER

K-Number: K960548 · 1996-04-26

ApplicantDentsply Intl.
Decision Date1996-04-26
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AH PLUS ROOT CANAL SEALER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1996-04-26 under 510(k) number K960548. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AH PLUS ROOT CANAL SEALER?

AH PLUS ROOT CANAL SEALER is a medical device that received FDA 510(k) clearance on 1996-04-26. The listed applicant is Dentsply Intl.. The 510(k) number is K960548.

When did AH PLUS ROOT CANAL SEALER receive FDA 510(k) clearance?

AH PLUS ROOT CANAL SEALER received FDA 510(k) clearance on 1996-04-26, under 510(k) number K960548.

Who is the listed applicant for AH PLUS ROOT CANAL SEALER?

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 AH PLUS ROOT CANAL SEALER?

The FDA product code for AH PLUS ROOT CANAL SEALER is KIF.

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Related Devices (Code: KIF)

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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