Servo Nebulizer 945 Siemens-Elema AB

FDA 510(k) K871293 · Siemens Elema AB

Substantially Equivalent

510(k) numberK871293

Submission

Device name
Servo Nebulizer 945 Siemens-Elema AB
Applicant
Siemens Elema AB
Schaumburg, IL, US
Received
March 31, 1987
Decision date
May 8, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAF – Nebulizer (Direct Patient Interface)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5630
Specialty
Anesthesiology

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Questions and answers

When was Servo Nebulizer 945 Siemens-Elema AB cleared by the FDA?

Servo Nebulizer 945 Siemens-Elema AB (K871293) received a 510(k) decision of Substantially Equivalent on May 8, 1987, 38 days after the submission was received.

What is the product code of K871293?

The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.