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FDA 510(k)

EVIDENT MARK 2 APEX LOCATOR

K-Number: K863834 · 1987-02-06

ApplicantPulpdent Corp. of America
Decision Date1987-02-06
Product Code
DecisionSubstantially Equivalent

Device Summary

EVIDENT MARK 2 APEX LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Pulpdent Corp. of America. It received FDA 510(k) clearance on 1987-02-06 under 510(k) number K863834. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVIDENT MARK 2 APEX LOCATOR?

EVIDENT MARK 2 APEX LOCATOR is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Pulpdent Corp. of America. The 510(k) number is K863834.

When did EVIDENT MARK 2 APEX LOCATOR receive FDA 510(k) clearance?

EVIDENT MARK 2 APEX LOCATOR received FDA 510(k) clearance on 1987-02-06, under 510(k) number K863834.

Who is the listed applicant for EVIDENT MARK 2 APEX LOCATOR?

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

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Other records listing Pulpdent Corp. of America 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.

K882576ACID ETCH GELK854977FIBER MESHK844446BISICO SL(PUTTY) BISICO S2(REGULAR) S3 HEAVY ETC.K853447POLYCARB WATER SETK810545PCA PERIOCARE PERIODONTAL DRESSING

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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