DIGITAL IMAGER— 510(k) K032022

Substantially Equivalent

Pyramid Medical, Inc.

FDA 510(k) clearance K032022 for DIGITAL IMAGER, Substantially Equivalent on 2003-09-02. Applicant: Pyramid Medical, Inc.. Device class: 2.

Clearance details

Applicant: Pyramid Medical, Inc.
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 2003-06-30
Decision date: 2003-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Alamitos, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LMA

K132183 — DICOM VIDEO2013-10-03
K130636 — TELERADPRO EDGE; TELERADPRO EDGE HD-CCD2013-06-07
K130406 — DIAGNOSTICPRO EDGE2013-04-29
K102476 — TELERADPRO2010-10-07
K093809 — VIDAR DENTAL FILM DIGITIZER2010-01-07

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