FDA 510(k)

R&R ALSTON CARBIDE BURS

K-Number: K771347 · 1977-08-03

Decision Date1977-08-03

Product CodeEJL

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

R&R ALSTON CARBIDE BURS 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 1977-08-03 under 510(k) number K771347. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&R ALSTON CARBIDE BURS?

R&R ALSTON CARBIDE BURS is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Ransom and Randolph. The 510(k) number is K771347.

When did R&R ALSTON CARBIDE BURS receive FDA 510(k) clearance?

R&R ALSTON CARBIDE BURS received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771347.

Who is the listed applicant for R&R ALSTON CARBIDE BURS?

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

What is the FDA product code for R&R ALSTON CARBIDE BURS?

The FDA product code for R&R ALSTON CARBIDE BURS is EJL.

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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 K770598ENDODONTIC INSTRUMENTS, R&R CUTWELL K761067DENTSPLY DIE STONE

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Related Devices (Code: EJL)

K080687SMARTBURSS.S. White Burs, Inc.K071352CERADRILLGebr. Brasseler GmbH & Co. KG K061383BTI STERILE DENTAL DRILLS KIT, BTI ABUTMENTS AND CAPSB.T.I. Biotechnology Institute, Sl.K943273TRI HAWK BUR, FG BURTri Hawk Corp.K926205MONOSTERYLUtensili Super Abrasivi K923883DENTAL OR SURGICAL BURStratum Dental Technologies, Inc.

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.