Spacelabs Medical Multiparameter Module 91496

by Spacelabs Medical, Inc. 510(k)

Active United States

510(k) K050175

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK050175	Date4 Mar 2005Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
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: K050175
FDA Product Code: DSI

Device Class: Class II
Regulation: 21 CFR Part 870.1025
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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