ClearanceBrief
Company ยท US

Egnell, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1985. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BTAPump, Portable, Aspiration (Manual Or Powered)5
FMTWarmer, Infant Radiant1
FMZIncubator, Neonatal1
FRNPump, Infusion1
HGXPump, Breast, Powered1
LBIUnit, Neonatal Phototherapy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 25, 1985K853917EGNELL COMPACT SUCTION PUMP
Egnell, Inc.
BTA
Nov 25, 1985K853909EGNELL UNIVERSAL SUCTION PUMP
Egnell, Inc.
BTA
Feb 4, 1985K844307EGNELL-LACT B BATTERY-OPERATED BREAST PUMP
Egnell, Inc.
HGX
Apr 30, 1984K840526AMETHERM
Egnell, Inc.
FMZ
Apr 20, 1984K834335AMEDA PHOTOTHERAPY LAMP FOR NEWBORN
Egnell, Inc.
LBI
Dec 22, 1983K832637AMEDA NEONATAL RESUSCITATION UNIT-
Egnell, Inc.
FMT
Dec 31, 1981K813312UNIVERSAL SUCTION PUMP TYPE EUS
Egnell, Inc.
BTA
Dec 9, 1981K813095GASTRIC JUICES SUCTION PUMP
Egnell, Inc.
BTA
Dec 2, 1981K812898PE-01 ELECTRONIC INFUSION PUMP
Egnell, Inc.
FRN
Oct 20, 1981K812020EGNELL COMPACT, TYPE EHV
Egnell, Inc.
BTA

Latest recalls

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