ClearanceBrief
Company ยท US

E. Benson Hood Laboratories, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1999. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BTOTube, Tracheostomy (W/Wo Connector)1
EOQBronchoscope (Flexible Or Rigid)1
FWNProsthesis, Larynx (Stents And Keels)1
KNTTubes, Gastrointestinal (And Accessories)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 29, 1999K983878CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE
E. Benson Hood Laboratories, Inc.
EOQ
Jul 26, 1984K841350SALIVARY BYPASS TUBE
E. Benson Hood Laboratories, Inc.
Jul 23, 1984K841349ESOPHAGEAL TUBE
E. Benson Hood Laboratories, Inc.
KNT
Jun 14, 1984K841266MONTGOMERY TRACHEAL T-TUBE
E. Benson Hood Laboratories, Inc.
BTO
May 2, 1984K841348UMBRELLA KEEL
E. Benson Hood Laboratories, Inc.
May 2, 1984K841347LARYNGEAL STENT
E. Benson Hood Laboratories, Inc.
FWN

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes