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FDA 510(k)

SANICURE DISPOSABLE CURING PROBE

K-Number: K962405 · 1996-08-29

Decision Date1996-08-29
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SANICURE DISPOSABLE CURING PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Efos Canada, Inc.. It received FDA 510(k) clearance on 1996-08-29 under 510(k) number K962405. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANICURE DISPOSABLE CURING PROBE?

SANICURE DISPOSABLE CURING PROBE is a medical device that received FDA 510(k) clearance on 1996-08-29. The listed applicant is Efos Canada, Inc.. The 510(k) number is K962405.

When did SANICURE DISPOSABLE CURING PROBE receive FDA 510(k) clearance?

SANICURE DISPOSABLE CURING PROBE received FDA 510(k) clearance on 1996-08-29, under 510(k) number K962405.

Who is the listed applicant for SANICURE DISPOSABLE CURING PROBE?

The FDA 510(k) record lists Efos Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SANICURE DISPOSABLE CURING PROBE?

The FDA product code for SANICURE DISPOSABLE CURING PROBE is EBF.

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.

Related Devices (Code: EBF)

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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