SFD-035 SPOT FILM DEVICE— 510(k) K902146

Substantially Equivalent

Rms Div.

FDA 510(k) clearance K902146 for SFD-035 SPOT FILM DEVICE, Substantially Equivalent on 1990-05-31. Applicant: Rms Div.. Device class: 2.

Clearance details

Applicant: Rms Div.
Product code: Code IXL
Device class: Class 2
Regulation: 21 CFR 892.1670
Advisory panel: Radiology
Date received: 1990-05-14
Decision date: 1990-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Addison, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXL

K111304 — OPTIMA XR1202011-07-19
K964806 — MD-18351997-03-04
K950317 — ADVANTX 1824 SPOTFILM DEVICE1995-02-08
K940386 — KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP1994-08-17
K942367 — AXT 1400 SPOTFILM DEVICE1994-06-06

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
K941625 — DW234 #291994-06-22

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