ClearanceBrief
Company ยท US

Richard-Allan Medical

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1994. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEIElectrosurgical, Cutting & Coagulation & Accessories2
FSMTray, Surgical, Instrument1
GAGStapler, Surgical1
GEFApplier, Staple, Surgical,1
HBTApplier, Hemostatic Clip1
HIFInsufflator, Laparoscopic1
KKXDrape, Surgical, Antimicrobial1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 27, 1994K942207REFLEX INS INSUFFLATION NEEDLE
Richard-Allan Medical
HIF
Feb 22, 1994K935105REFLEX ESP WITH FINGER SWITCHES
Richard-Allan Medical
GEI
Nov 23, 1993K933508REFLEX SDD SURGICAL STAPLER
Richard-Allan Medical
GEF
Nov 19, 1993K933901REFLEX(R) EHS (ENDOSCOPIC HERNIA STAPLER)
Richard-Allan Medical
GAG
Jul 23, 1993K924881REFLEX(R) ESP
Richard-Allan Medical
GEI
Jul 21, 1993K924929REFLEX(R) ECA
Richard-Allan Medical
HBT
Feb 19, 1991K905701RICHARD-ALLAN SHEET CLIP
Richard-Allan Medical
KKX
Feb 19, 1991K905682RICHARD-ALLAN CLAMP COVERS
Richard-Allan Medical
FSM

Latest recalls

DateFirm and productCodeLinked 510(k)
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