Cleared Traditional

STRAIGHT CONNECTORS, 22MM

K860886 · Dhd Medical Products Div. Diemolding Corp. · Anesthesiology

Mar 1986

Decision

22d

Days

Class 1

Risk

About This 510(k) Submission

K860886 is an FDA 510(k) clearance for the STRAIGHT CONNECTORS, 22MM, a Connector, Airway (extension) (Class I — General Controls, product code BZA), submitted by Dhd Medical Products Div. Diemolding Corp. (Canastota, US). The FDA issued a Cleared decision on March 19, 1986, 22 days after receiving the submission on February 25, 1986. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5810.

Submission Details

510(k) Number	K860886 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 25, 1986
Decision Date	March 19, 1986
Days to Decision	22 days
Submission Type	Traditional
Review Panel	Anesthesiology (AN)
Summary	—