Cleared Traditional

K932588 - PEDIATRIC TEMPERATURE MONITORING CIRCUITS (FDA 510(k) Clearance)

Jul 1993
Decision
55d
Days
Class 1
Risk

K932588 is an FDA 510(k) clearance for the PEDIATRIC TEMPERATURE MONITORING CIRCUITS. This device is classified as a Circuit, Breathing (w Connector, Adaptor, Y Piece) (Class I - General Controls, product code CAI).

Submitted by Merit Medical Systems, Inc. (Indianapolis, US). The FDA issued a Cleared decision on July 21, 1993, 55 days after receiving the submission on May 27, 1993.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5240.

Submission Details

510(k) Number K932588 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 27, 1993
Decision Date July 21, 1993
Days to Decision 55 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement

Device Classification

Product Code CAI — Circuit, Breathing (w Connector, Adaptor, Y Piece)
Device Class Class I - General Controls
CFR Regulation 21 CFR 868.5240