ClearanceBrief
Company ยท US

Acra Cut, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 2003. 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
HBFDrills, Burrs, Trephines & Accessories (Compound, Powered)3
HAOInstrument, Surgical, Non-Powered2
HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)2
HBOClip, Scalp1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 8, 2003K032970ACRA-CUT XPRESS 120
Acra Cut, Inc.
HBF
Nov 18, 1994K944311ACRA-CUT
Acra Cut, Inc.
HBO
Sep 10, 1991K911819ACRA-CUT NEUROLOGICAL SURGICAL DEVICE-POWERED
Acra Cut, Inc.
HBE
Sep 10, 1991K911812ACRA-CUT WIRE PASS DRILL
Acra Cut, Inc.
HBE
Feb 12, 1991K910226DURAL DISSECTORS
Acra Cut, Inc.
HAO
Feb 12, 1991K910225BONE PAD REMOVER
Acra Cut, Inc.
HAO
Jun 15, 1989K892866AUTOMATIC CRANIAL DRILL (PERFORATOR)
Acra Cut, Inc.
HBF
Dec 29, 1983K833266ACRA-CUT
Acra Cut, Inc.
HBF

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes