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The Nomos Minicrane

by Nomos Corp.

510(k) K964740

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK964740 Date11 Feb 1997ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
JAI
Device Class
Class II
Regulation
21 CFR Part 892.5770
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 26 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Nomos Minicrane is a mechanical accessory for radiation therapy patient support assemblies. It attaches to table side rails or fixation devices like the NOMOGrip and features an arm of variable length with a battery-operated digital micrometer.

The device is supplied as a Class II medical device with FDA 510(k) clearance (K964740) and is intended for use in radiology. It is regulated under product code JAI and classification name Couch, Radiation Therapy, Powered, with a decision date of 1997-02-11.

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