ROOT CANAL FILLING APPLICATOR NEEDLES— 510(k) K801484

Name: FDA 510(k) clearance K801484
Creator: U.S. Food and Drug Administration
Published: 1980-07-21

Substantially Equivalent

National Patent Development Corp.

FDA 510(k) clearance K801484 for ROOT CANAL FILLING APPLICATOR NEEDLES, Substantially Equivalent on 1980-07-21. Applicant: National Patent Development Corp.. Device class: 1.

Clearance details

Applicant: National Patent Development Corp.
Product code: Code EIC
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1980-05-16
Decision date: 1980-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIC

view all

K972234 — RCT GEL ROOT CANAL THERAPY GEL1997-06-30
K864307 — MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)1986-11-18
K861846 — HYDRON ROOT CANAL FILLING & MARK IV STARTER KIT1986-06-26
K851944 — MAX-I-PROBE HANDPIECE1985-07-01
K840237 — MAX-I-PROBE PERIODONTAL ENDODONTIC PROB1984-04-05

More clearances from National Patent Development Corp.

view all

K843974 — VARIABLE TEMPERATURE CAUTERY DEVICE1985-02-26
K832699 — HYDRON WOUND DRESSING FAST SEAT KIT1984-04-27
K822793 — PIO ROOT CANAL INDICATOR1982-10-22
K820028 — ZEON COMPOSITE RESIN LIGHT CURE SYS1982-03-11
K820006 — ZEON COMPOSITE RESIN SYSTEM1982-01-22

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