MOTI APRON— 510(k) K810095

Substantially Equivalent

Moti Enterprises, Inc.

FDA 510(k) clearance K810095 for MOTI APRON, Substantially Equivalent on 1981-02-12. Applicant: Moti Enterprises, Inc.. Device class: 1.

Clearance details

Applicant: Moti Enterprises, Inc.
Product code: Code KPY
Device class: Class 1
Regulation: 21 CFR 892.6500
Advisory panel: Radiology
Date received: 1981-01-14
Decision date: 1981-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPY

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K953610 — AUKULYTE1995-09-26

More clearances from Moti Enterprises, Inc.

K843437 — MEI MAMMOGRAPHY SYS MX-20491984-11-27
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Data sourced from openFDA. This site is unofficial and independent of the FDA.