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FDA 510(k)

EDENTRACE MULTI-CHARTER MODEL 3700

K-Number: K883315 · 1988-12-28

ApplicantEdentec Corp.
Decision Date1988-12-28
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EDENTRACE MULTI-CHARTER MODEL 3700 is the device name listed in this FDA 510(k) record. The listed applicant is Edentec Corp.. It received FDA 510(k) clearance on 1988-12-28 under 510(k) number K883315. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EDENTRACE MULTI-CHARTER MODEL 3700?

EDENTRACE MULTI-CHARTER MODEL 3700 is a medical device that received FDA 510(k) clearance on 1988-12-28. The listed applicant is Edentec Corp.. The 510(k) number is K883315.

When did EDENTRACE MULTI-CHARTER MODEL 3700 receive FDA 510(k) clearance?

EDENTRACE MULTI-CHARTER MODEL 3700 received FDA 510(k) clearance on 1988-12-28, under 510(k) number K883315.

Who is the listed applicant for EDENTRACE MULTI-CHARTER MODEL 3700?

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

What is the FDA product code for EDENTRACE MULTI-CHARTER MODEL 3700?

The FDA product code for EDENTRACE MULTI-CHARTER MODEL 3700 is DSF.

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 Edentec 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 18 devices →

Related Devices (Code: DSF)

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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