ClearanceBrief
Company ยท US

Autovage

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1992. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KDHCatheter (Gastric, Colonic, Etc.), Irrigation And Aspiration4
BTRTube, Tracheal (W/Wo Connector)1
EYFProtector, Wound, Plastic1
KNTTubes, Gastrointestinal (And Accessories)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 16, 1992K922785IRRIVAGE
Autovage
EYF
Apr 13, 1992K914908QUICVAGE PLUS
Autovage
KDH
Jan 24, 1992K914907QUICVAGE
Autovage
KDH
Jul 26, 1991K911919MINIVAGE(R)
Autovage
KDH
Jul 26, 1991K911788ECONOVAGE R
Autovage
KDH
May 25, 1984K840943ENDO-JECT
Autovage
BTR
Dec 3, 1982K823195GASTRIC LAVAGE KIT
Autovage
KNT

Latest recalls

DateFirm and productCodeLinked 510(k)
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