Skip to content

Blease Sirius Anesthesia System, Models 3000 and 2000

by Blease Medical Equipment, Ltd. 510(k)

Active United States

510(k) K041430

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK041430 Date7 Oct 2004ClearedStatusActive

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  • Withdrawn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
BSZ
FDA applicant
Blease Medical Equipment , Ltd.
Device Class
Class II
Regulation
21 CFR Part 868.5160
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Other devices from Blease Medical Equipment, Ltd.