Model 330 Multifunction Aspirator

FDA 510(k) K170533 · ZOLL Medical Corporation

Substantially Equivalent

510(k) numberK170533

Submission

Device name
Model 330 Multifunction Aspirator
Applicant
ZOLL Medical Corporation
Chelsmford, MA, US
Received
February 23, 2017
Decision date
April 18, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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Questions and answers

When was Model 330 Multifunction Aspirator cleared by the FDA?

Model 330 Multifunction Aspirator (K170533) received a 510(k) decision of Substantially Equivalent on April 18, 2017, 54 days after the submission was received.

What is the product code of K170533?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.