ClearanceBrief
Company ยท US

Bip USA, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2003. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GDFGuide, Needle, Surgical2
KNWInstrument, Biopsy2
FCGBiopsy Needle1
MDMInstrument, Manual, Surgical, General Use1
MJGDevice, Percutaneous, Biopsy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 11, 2003K024089VACUFLASH BIOPSY SYSTEM
Bip USA, Inc.
KNW
Apr 28, 1994K934371BIP MULTI MODIFICATION
Bip USA, Inc.
KNW
Mar 7, 1994K934370BIP BIOPSY NEEDLE MODIFICATION
Bip USA, Inc.
FCG
Feb 17, 1994K935457LOCALIZATION WIRE OR MARKER - SURGICAL
Bip USA, Inc.
GDF
May 19, 1993K925870SPACER
Bip USA, Inc.
MJG
Apr 6, 1993K925875HORIZONTAL NEEDLE GUIDE ATTACHMENT
Bip USA, Inc.
GDF
Mar 16, 1993K925874BREAST STABILIZER
Bip USA, Inc.
MDM

Latest recalls

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