Vacpac Portable Aspiration System

FDA 510(k) K910271 · Jedmed Instrument Co.

Substantially Equivalent

510(k) numberK910271

Submission

Device name
Vacpac Portable Aspiration System
Applicant
Jedmed Instrument Co.
St.Louis, MO, US
Received
January 23, 1991
Decision date
March 20, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Vacpac Portable Aspiration System cleared by the FDA?

Vacpac Portable Aspiration System (K910271) received a 510(k) decision of Substantially Equivalent on March 20, 1991, 56 days after the submission was received.

What is the product code of K910271?

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