Microaire Power Aspiration Device Pad System

FDA 510(k) K973268 · Microaire Surgical Instruments, Inc.

Substantially Equivalent

510(k) numberK973268

Submission

Device name
Microaire Power Aspiration Device Pad System
Applicant
Microaire Surgical Instruments, Inc.
Charlottesville, VA, US
Received
August 29, 1997
Decision date
November 26, 1997
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 Microaire Power Aspiration Device Pad System cleared by the FDA?

Microaire Power Aspiration Device Pad System (K973268) received a 510(k) decision of Substantially Equivalent on November 26, 1997, 89 days after the submission was received.

What is the product code of K973268?

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