Cleared Traditional

K932094 - BOVIE ULTRASONIC SURGICAL ASPIRATOR
(FDA 510(k) Clearance)

K932094 · Mdt Corp., Inc. · General & Plastic Surgery device

Jul 1993

Decision

82d

Days

—

Risk

K932094 is an FDA 510(k) clearance for the BOVIE ULTRASONIC SURGICAL ASPIRATOR. This device is classified as a Instrument, Ultrasonic Surgical.

Submitted by Mdt Corp., Inc. (Salt Lake City, US). The FDA issued a Cleared decision on July 21, 1993, 82 days after receiving the submission on April 30, 1993.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number	K932094 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	April 30, 1993
Decision Date	July 21, 1993
Days to Decision	82 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	Summary PDF