ClearanceBrief
Company ยท US

Gyneco, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1986. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRMCompressor, Cardiac, External1
HFBForceps, Biopsy, Gynecological1
HFEBrush, Endometrial1
HHKCurette, Suction, Endometrial (And Accessories)1
LDFElectrode, Pacemaker, Temporary1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 5, 1986K861409SYNCARE TEMPORARY CARDIAC PACING WIRE
Gyneco, Inc.
LDF
Apr 2, 1986K853216MASTER ENDOMET BIOPSY KIT W/PLAS CURE 3,4MM-4003,4
Gyneco, Inc.
HHK
Jul 5, 1985K852357GYNE-SHEAR CERVICAL BIOPSY INSTRUMENT W/DISPIS TIP
Gyneco, Inc.
HFB
Feb 25, 1985K843941ENDOCYTE
Gyneco, Inc.
HFE
Aug 17, 1984K841275FINE NEEDLE ASPIRATION DEVICE
Gyneco, Inc.
DRM

Latest recalls

DateFirm and productCodeLinked 510(k)
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