ADMARK— 510(k) K923533

Substantially Equivalent

Planmeca USA, Inc.

FDA 510(k) clearance K923533 for ADMARK, Substantially Equivalent on 1993-03-04. Applicant: Planmeca USA, Inc.. Device class: 1.

Clearance details

Applicant: Planmeca USA, Inc.
Product code: Code JAC
Device class: Class 1
Regulation: 21 CFR 892.1640
Advisory panel: Radiology
Date received: 1992-07-16
Decision date: 1993-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Finland, FI

Download summary PDF View on FDA.gov ↗

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K926404 — KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4L1993-03-04

More clearances from Planmeca USA, Inc.

K111361 — PLANMED NUANCE EXCEL2011-09-23
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K923534 — PM2002 PROLINE1994-01-31
K923461 — PM2002 PROLINE, PM2002 PROLINE EC1992-12-21
K923462 — DELIGHT1992-12-21

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