Cleared Traditional

PRECISION MEDICAL ELIMINATOR

K902917 · Precision Medical, Inc. · Anesthesiology
Jul 1990
Decision
20d
Days
Class 1
Risk

About This 510(k) Submission

K902917 is an FDA 510(k) clearance for the PRECISION MEDICAL ELIMINATOR, a Flowmeter, Calibration, Gas (Class I — General Controls, product code BXY), submitted by Precision Medical, Inc. (Northampton, US). The FDA issued a Cleared decision on July 23, 1990, 20 days after receiving the submission on July 3, 1990. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.2350.

Submission Details

510(k) Number K902917 FDA.gov
FDA Decision Cleared SESE
Date Received July 03, 1990
Decision Date July 23, 1990
Days to Decision 20 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary —

Device Classification

Product Code BXY — Flowmeter, Calibration, Gas
Device Class Class I — General Controls
CFR Regulation 21 CFR 868.2350