Cpi, MAXI-VAC(6480),THOMAS Industries, MEDI-PUMP(1240/1242/1243)

FDA 510(k) K965059 · Thomas Industries

Substantially Equivalent

510(k) numberK965059

Submission

Device name
Cpi, MAXI-VAC(6480),THOMAS Industries, MEDI-PUMP(1240/1242/1243)
Applicant
Thomas Industries
Sheboygan, WI, US
Received
December 18, 1996
Decision date
March 4, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Cpi, MAXI-VAC(6480),THOMAS Industries, MEDI-PUMP(1240/1242/1243) cleared by the FDA?

Cpi, MAXI-VAC(6480),THOMAS Industries, MEDI-PUMP(1240/1242/1243) (K965059) received a 510(k) decision of Substantially Equivalent on March 4, 1997, 76 days after the submission was received.

What is the product code of K965059?

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