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FDA 510(k)

VAPAMASTA 5

K-Number: K884686 · 1989-03-15

ApplicantDentsply Intl.
Decision Date1989-03-15
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VAPAMASTA 5 is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K884686. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAPAMASTA 5?

VAPAMASTA 5 is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Dentsply Intl.. The 510(k) number is K884686.

When did VAPAMASTA 5 receive FDA 510(k) clearance?

VAPAMASTA 5 received FDA 510(k) clearance on 1989-03-15, under 510(k) number K884686.

Who is the listed applicant for VAPAMASTA 5?

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 VAPAMASTA 5?

The FDA product code for VAPAMASTA 5 is CAD.

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Related Devices (Code: CAD)

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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