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Alu-Kart

by Micro Encapsulation Tech.

510(k) K841178

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 11 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 11 Oct 2026. What this means

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESP Substantially Equivalent — Postmarket Surveillance · Traditional NumberK841178 Date20 Mar 1984ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 11 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  • Withdrawn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
Advisory Committee
Unknown
FDA Decision
SESP Substantially Equivalent — Postmarket Surveillance

Other devices from Micro Encapsulation Tech.

  • Dia-Kart

    Not classified

  • Hemo-Kart

    Not classified