Medical Device Manufacturer · US , Washington , DC

Roseburg SA - FDA 510(k) Cleared Devices

24 submissions · 23 cleared · Since 1985

Total

Cleared

Denied

Roseburg SA has 23 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 23 cleared submissions from 1985 to 1994.

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

Roseburg SA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Roseburg SA

24 devices

1-12 of 24

Cleared Sep 01, 1994

STAPLE, FIXATION BONE

K931155 · HWC

Orthopedic · 541d

Cleared Mar 09, 1989

CALIUS-ISABEL CANOVAS SUNGLASSES

K890081 · HQY

Ophthalmic · 58d

Cleared Jan 24, 1989

ASSENAT-BLESCHET SUNGLASSES

K885275 · HQY

Ophthalmic · 28d

Cleared Aug 26, 1988

BURNET LABORATOIRE PHARMACEUTIQUE SURGICAL GLOVES

K882392 · KGO

General Hospital · 77d

Cleared Dec 07, 1987

UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERY

K872715 · JDN

Orthopedic · 150d

Cleared Nov 17, 1987

POIRIER KID-ROLLER MANUAL WHEELCHAIR

K874317 · IOR

Physical Medicine · 27d

Cleared Jul 21, 1987

S.T.A.C.E.M. EXTERNAL BREAST PROSTHESIS MAMMARY

K872714 · GBI

General & Plastic Surgery · 11d

Cleared May 29, 1987

SPECTACLE FRAME - DANIELLE

K871688 · HQZ

Ophthalmic · 30d

Cleared May 29, 1987

SPECTACLE FRAME - LORRAINE

POIRIER POWERED WHEELCHAIR

K864791 · ITI

Physical Medicine · 58d

Roseburg SA - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Roseburg SA

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