ENDODONTIC INSTRUMENTS, R&R CUTWELL— 510(k) K770598

Name: FDA 510(k) clearance K770598
Creator: U.S. Food and Drug Administration
Published: 1977-04-05

Substantially Equivalent

Ransom and Randolph

FDA 510(k) clearance K770598 for ENDODONTIC INSTRUMENTS, R&R CUTWELL, Substantially Equivalent on 1977-04-05. Applicant: Ransom and Randolph. Device class: 1.

Clearance details

Applicant: Ransom and Randolph
Product code: Code EKP
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1977-03-29
Decision date: 1977-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code EKP

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K823686 — REAMER TYPE K ENDODONTIC1982-12-28
K822620 — ROOT CANAL REAMERS, TYPE K1982-09-28
K800291 — ENDEX REAMERS PULP CANAL, ENDODONTIC1980-02-19
K770331 — DIALYSIS, JET SYSTEM1977-04-20
K770367 — ROOT CANAL FILES & REAMERS1977-03-01

More clearances from Ransom and Randolph

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K781605 — R&R ABSORBENT POINTS1978-10-10
K780399 — INSTRUMENT CLEANING BRUSH1978-03-17
K780198 — PROPHY CUPS, R&R1978-02-16
K780199 — PROPHY ANGLES, R&R1978-02-16
K771347 — R&R ALSTON CARBIDE BURS1977-08-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.