Medi-Pump Aspirator, Model 1615

FDA 510(k) K041199 · Thomas Industries

Substantially Equivalent

510(k) numberK041199

Submission

Device name
Medi-Pump Aspirator, Model 1615
Applicant
Thomas Industries
Sheboygan, WI, US
Received
May 7, 2004
Decision date
June 1, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 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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K944399Medi-PumpBTA · Traditional 01/18/1995SE
K925010Nebulizer Pump, Powered, Model 1110BTI · Traditional 05/27/1994SE
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Questions and answers

When was Medi-Pump Aspirator, Model 1615 cleared by the FDA?

Medi-Pump Aspirator, Model 1615 (K041199) received a 510(k) decision of Substantially Equivalent on June 1, 2004, 25 days after the submission was received.

What is the product code of K041199?

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