Medical Device Manufacturer · US , Mchenry , IL

Richard-Allan Medical Ind., Inc. - FDA 510(k) Cleared Devices

33 submissions · 33 cleared · Since 1977

Total

Cleared

Denied

Richard-Allan Medical Ind., Inc. has 33 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 33 cleared submissions from 1977 to 1994.

Browse the FDA 510(k) cleared devices submitted by Richard-Allan Medical Ind., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Richard-Allan Medical Ind., Inc.

33 devices

1-12 of 33

Cleared Mar 24, 1994

REFLEX HTR

K931879 · GCJ

General & Plastic Surgery · 344d

Cleared Feb 22, 1994

REFLEX(R) ESC

K924200 · KNF

Obstetrics & Gynecology · 551d

Cleared Oct 15, 1993

REFLEX ESI

K926297 · GEI

General & Plastic Surgery · 305d

Cleared Apr 20, 1993

STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD

K924761 · GCJ

General & Plastic Surgery · 209d

Cleared May 03, 1990

RICHARD-ALLAN VESSEL LOOPS

K900566 · KDC

General & Plastic Surgery · 85d

Cleared Jan 02, 1990

TITANIUM LIGATING CLIPS

K896262 · HBT

General & Plastic Surgery · 64d

Cleared Feb 27, 1989

PROTECTOR (SURGICAL INSTRUMENT)

K890314 · MMK

General Hospital · 35d

Cleared Nov 27, 1987

REFLEX(TM) CA-T CLIP APPLIER

K873309 · FZP

General & Plastic Surgery · 101d

Cleared Jul 23, 1986

REFLEX(TM) CLIP APPLIER

K862404 · FZP

General & Plastic Surgery · 28d

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2

Richard-Allan Medical Ind., Inc. - FDA 510(k) Cleared Devices

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