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I.V. Bottle (Ridgid)

by Medi-Plast Intl., Inc.

510(k) K811234

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

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 NumberK811234 Date18 Jun 1981ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-2641-2024 FDA Class II initiated 3 Jun 2024

    During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.

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  • Withdrawn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
KPE
Device Class
Class II
Regulation
21 CFR Part 880.5025
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

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