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Mdt Urology Table

by Mdt Corp., Inc.

510(k) K942485

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK942485 Date26 Aug 1994ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 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  • Withdrawn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
MMZ
Device Class
Class II
Regulation
21 CFR Part 876.4890
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 27 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 Mdt Urology Table is a cystometric, electric table used in medical settings. It is classified as a device with a product code of MMZ and is associated with the medical specialties of Gastroenterology and Urology. The device has a registration number and is subject to regulation under 876.4890. It is an electric table designed for urology procedures.

The Mdt Urology Table is supplied by Mdt Corp., Inc. and has been cleared under FDA 510(k) number K942485. The device is intended for use in a clinical setting and is subject to the regulations outlined in its clearance. The table is electric and has a specific product code, MMZ. It is classified as a class 2 device and has a unique set of registration numbers and a regulation number.

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