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FDA 510(k)

PULPDENT TOUCHDOWN

K-Number: K953217 · 1995-08-25

ApplicantPulpdent Corp.
Decision Date1995-08-25
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PULPDENT TOUCHDOWN is the device name listed in this FDA 510(k) record. The listed applicant is Pulpdent Corp.. It received FDA 510(k) clearance on 1995-08-25 under 510(k) number K953217. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULPDENT TOUCHDOWN?

PULPDENT TOUCHDOWN is a medical device that received FDA 510(k) clearance on 1995-08-25. The listed applicant is Pulpdent Corp.. The 510(k) number is K953217.

When did PULPDENT TOUCHDOWN receive FDA 510(k) clearance?

PULPDENT TOUCHDOWN received FDA 510(k) clearance on 1995-08-25, under 510(k) number K953217.

Who is the listed applicant for PULPDENT TOUCHDOWN?

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

What is the FDA product code for PULPDENT TOUCHDOWN?

The FDA product code for PULPDENT TOUCHDOWN is DYH.

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Other records listing Pulpdent 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.

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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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