Cleared Traditional

THAYER SUCTION EVACUATION CONDENSATE COLLECTION

K900047 · Thayer Medical Corp. · Anesthesiology
Apr 1990
Decision
110d
Days
Class 1
Risk

About This 510(k) Submission

K900047 is an FDA 510(k) clearance for the THAYER SUCTION EVACUATION CONDENSATE COLLECTION, a Drain, Tee (water Trap) (Class I — General Controls, product code BYH), submitted by Thayer Medical Corp. (Tucson, US). The FDA issued a Cleared decision on April 23, 1990, 110 days after receiving the submission on January 3, 1990. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5995.

Submission Details

510(k) Number K900047 FDA.gov
FDA Decision Cleared SESE
Date Received January 03, 1990
Decision Date April 23, 1990
Days to Decision 110 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary —

Device Classification

Product Code BYH — Drain, Tee (water Trap)
Device Class Class I — General Controls
CFR Regulation 21 CFR 868.5995

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