Medical Device Manufacturer · US , Mchenry , IL

Sybron Corp. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1977

Total

Cleared

Denied

Sybron Corp. has 37 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 37 cleared submissions from 1977 to 1986.

Browse the FDA 510(k) cleared devices submitted by Sybron Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sybron Corp.

37 devices

1-12 of 37

PROOF ALGINATE IMPRESSION MATERIAL

K854855 · ELW

Dental · 56d

Cleared Oct 25, 1984

DIAGNOSTIC MICROSOPCE SLIDES

K844092

Chemistry · 6d

Cleared Jul 18, 1984

TYCOS SELF-CHECK/DIGITAL FEVER THERMO

K842132 · FLL

General Hospital · 49d

Cleared Jul 13, 1984

KERR SEALAPEX ROOT CANAL SEALER

K841910 · EJK

Dental · 65d

Cleared Jun 05, 1984

LIEBEL-FLARSHEIM AFC 1000 X-RAY FILM

K841732 · IZP

Radiology · 40d

Cleared May 21, 1984

KERR RESIN BONDED BRIDGE CEMENT

K840407 · EMA

Dental · 111d

Cleared May 21, 1984

TYCOS SELF CHECK BPM3 BLOOD PRESS MONI

K840469 · DXN

Cardiovascular · 108d

Cleared Mar 05, 1984

LF MOTORIZED RADIOGRAPHIC FILM VIEWER

EVERBOND GLASS IONOMER CEMENT

K823795 · EMA

Dental · 30d

Cleared Oct 13, 1982

COMMAND BONDING RESIN/GLAZE/OPAQUER

K822869 · EBD

Dental · 16d

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Sybron Corp. - FDA 510(k) Cleared Devices

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