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FDA 510(k)

PROFESSIONAL MODEL 7525 DELIVERY SYSTEM

K-Number: K882759 · 1988-08-12

ApplicantViadent
Decision Date1988-08-12
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROFESSIONAL MODEL 7525 DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Viadent. It received FDA 510(k) clearance on 1988-08-12 under 510(k) number K882759. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFESSIONAL MODEL 7525 DELIVERY SYSTEM?

PROFESSIONAL MODEL 7525 DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-08-12. The listed applicant is Viadent. The 510(k) number is K882759.

When did PROFESSIONAL MODEL 7525 DELIVERY SYSTEM receive FDA 510(k) clearance?

PROFESSIONAL MODEL 7525 DELIVERY SYSTEM received FDA 510(k) clearance on 1988-08-12, under 510(k) number K882759.

Who is the listed applicant for PROFESSIONAL MODEL 7525 DELIVERY SYSTEM?

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

What is the FDA product code for PROFESSIONAL MODEL 7525 DELIVERY SYSTEM?

The FDA product code for PROFESSIONAL MODEL 7525 DELIVERY SYSTEM is EFS.

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Related Devices (Code: EFS)

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

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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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