FDA 510(k)

DENTSPLY DIE STONE

K-Number: K761067 · 1976-11-30

Decision Date1976-11-30

Product Code

DecisionSubstantially Equivalent

Device Summary

DENTSPLY DIE STONE is the device name listed in this FDA 510(k) record. The listed applicant is Ransom and Randolph. It received FDA 510(k) clearance on 1976-11-30 under 510(k) number K761067. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTSPLY DIE STONE?

DENTSPLY DIE STONE is a medical device that received FDA 510(k) clearance on 1976-11-30. The listed applicant is Ransom and Randolph. The 510(k) number is K761067.

When did DENTSPLY DIE STONE receive FDA 510(k) clearance?

DENTSPLY DIE STONE received FDA 510(k) clearance on 1976-11-30, under 510(k) number K761067.

Who is the listed applicant for DENTSPLY DIE STONE?

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

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Other records listing Ransom and Randolph as applicant

K781605R&R ABSORBENT POINTS K780399INSTRUMENT CLEANING BRUSH K780198PROPHY CUPS, R&R K780199PROPHY ANGLES, R&R K771347R&R ALSTON CARBIDE BURS K770598ENDODONTIC INSTRUMENTS, R&R CUTWELL

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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.