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AMT Capsule Dome G-Tube 9-CG2020

by Applied Medical Technology, Inc. 2 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842071111687 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not in commercial distribution

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  • Withdrawn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 — GUDID listing Listed

Specification

GUDID

Trade Name
AMT Capsule Dome G-Tube
Generic Name
Gastrostomy tube
Model / Reference
9-CG2020
Primary DI / UDI-DI
00842071111687
510(k) Number
FDA Product Code
KNT
GMDN Term
Gastrostomy tube
Device Class
Class II
Regulation Number
876.5980
GUDID distribution status
Not in Commercial Distribution
Size
Catheter Gauge — 20 French

Related devices

Cleared under the same submission (K043027)

Show all (12)

Other devices from Applied Medical Technology, Inc.

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No