DW234 #29— 510(k) K941625

Substantially Equivalent

Rms Div.

FDA 510(k) clearance K941625 for DW234 #29, Substantially Equivalent on 1994-06-22. Applicant: Rms Div.. Device class: 2.

Clearance details

Applicant: Rms Div.
Product code: Code EJS
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 1994-04-04
Decision date: 1994-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJS

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More clearances from Rms Div.

K963367 — RMS K-WIRE1996-10-30
K954438 — SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE1995-12-29
K944848 — THE VIVACARE T.P.S. PROBE1994-12-14
K944557 — DW250 #911994-11-03
K902403 — ELITE R/F SPOT FILM DRIVE1990-08-01

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