ClearanceBrief
Company ยท US

Ovamed Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 1995. 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
LKFCannula, Manipulator/Injector, Uterine2
HIHHysteroscope (And Accessories)1
MOVCatheters, Salpingography1
ODFMini Endoscope, Gastroenterology-Urology1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 20, 1995K951946HYSTEROSYS FLEXIBLE HYSTEROCOPE
Ovamed Corp.
HIH
Jul 28, 1995K931534OVAMED INTRAUTERINE ACCESS CATHETER
Ovamed Corp.
MOV
Jun 22, 1995K931167OVAMED FALLOPIAN OSTIAL ACCESS CATHETER
Ovamed Corp.
LKF
Mar 22, 1995K943593SARATOGA MODULAR MINIATURE ENDOSCOPE SYSTEM
Ovamed Corp.
ODF
Jan 30, 1995K931122OVAMED HSG CATHETER
Ovamed Corp.
LKF

Latest recalls

DateFirm and productCodeLinked 510(k)
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