VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)— 510(k) K050362

Name: FDA 510(k) clearance K050362
Creator: U.S. Food and Drug Administration
Published: 2005-03-15

Substantially Equivalent

Vident

FDA 510(k) clearance K050362 for VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES), Substantially Equivalent on 2005-03-15. Applicant: Vident. Device class: 2.

Clearance details

Applicant: Vident
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2005-02-14
Decision date: 2005-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

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K063768 — TITANIUM SCALLOPED ABUTMENT2007-06-27
K060441 — VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX982006-04-27
K052710 — VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,2006-01-13
K052130 — VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL402005-08-15
K022996 — VITA IN-CERAM YZ CUBES FOR CEREC2002-10-09

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