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Reprocessed RD SET Adt Pulse Oximeter Sensor (4000) +3 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K241758

by Stryker Sustainability Solutions

Identifiers

510(k) Number
K241758 FDA 510(k)
FDA Product Code
NLF FDA 510(k)
Models / Variants
Reprocessed RD SET Adt Pulse Oximeter Sensor (4000) FDA 510(k)
Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001) FDA 510(k)
Reprocessed RD SET Inf Pulse Oximeter Sensor (4002) FDA 510(k)
Reprocessed RD SET Adt Pulse Oximeter Sensor (4003) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 870.2700 FDA 510(k)
Regulation Number
870.2700 FDA 510(k)
Advisory Committee
Cardiovascular FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Reprocessed RD SET Adt Pulse Oximeter Sensor (4000) +3 more models by Stryker Sustainability Solutions — Class II — FDA_510K — listed in FDA 510(k) — 4 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Stryker Sustainability Solutions

Sources (1)

  • FDA 510(k) K241758 24 fields · synced Jun 18, 2026