ClearanceBrief
Company ยท US

Acuderm, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1994. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JSJCulture Media, Selective And Non-Differential3
MDMInstrument, Manual, Surgical, General Use2
FMFSyringe, Piston1
FMINeedle, Hypodermic, Single Lumen1
FYDApparatus, Exhaust, Surgical1
FZSCurette, Surgical, General Use1
GEXPowered Laser Surgical Instrument1
LROGeneral Surgery Tray1
LRYPunch, Surgical1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 24, 1994K933516ACU-E PUNCH
Acuderm, Inc.
LRY
Mar 7, 1994K933265ACU-DISPO-CE(TM)
Acuderm, Inc.
MDM
Feb 22, 1994K933137ACU-SUTURE KIT
Acuderm, Inc.
LRO
Feb 9, 1994K930043ACU-EVAC
Acuderm, Inc.
FYD
Dec 1, 1993K933866ACU-HEMOSTATIC RING
Acuderm, Inc.
MDM
Jan 27, 1992K915000ACU-GUARD
Acuderm, Inc.
GEX
Apr 11, 1989K891334ACU-CURETTE
Acuderm, Inc.
FZS
Nov 23, 1987K874024ACU-MICRO-NEEDLE
Acuderm, Inc.
FMI
Feb 19, 1986K854877ACU-SYRINGE W/WO NEEDLES
Acuderm, Inc.
FMF
Sep 12, 1983K832583SABOURAUD DEXTROSE AGAR
Acuderm, Inc.
JSJ
Sep 12, 1983K832582MYCOSEL AGAR
Acuderm, Inc.
JSJ
Sep 12, 1983K832581DTM-DERMATOPHYTE TEST MEDIUM
Acuderm, Inc.
JSJ
Jul 7, 1983K831635ACU-PUNCH
Acuderm, Inc.

Latest recalls

DateFirm and productCodeLinked 510(k)
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