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Merivaara Crib Trolley-Model 381

by Daun International, Inc. 510(k)

Active United States

510(k) K852173

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK852173 Date17 Jun 1985ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
FMS
Device Class
Class II
Regulation
21 CFR Part 880.5140
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

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