ClearanceBrief
Company ยท US

Conceptus, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1998. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HIHHysteroscope (And Accessories)2
LKFCannula, Manipulator/Injector, Uterine2
MKOFalloposcope2
HETLaparoscope, Gynecologic (And Accessories)1
MFDCannula, Intrauterine Insemination1
MOVCatheters, Salpingography1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 21, 1998K974028STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBING
Conceptus, Inc.
MKO
Sep 5, 1997K972210RESECTOSCOPE SAFETY SHEATH
Conceptus, Inc.
HIH
Jan 31, 1997K962587CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEM
Conceptus, Inc.
MKO
Mar 12, 1996K954164HYSTEROSCOPE
Conceptus, Inc.
HIH
Jul 28, 1995K953314CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM
Conceptus, Inc.
MOV
Mar 6, 1995K932387CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL
Conceptus, Inc.
HET
Jan 6, 1995K932993INTRAUTERINE CATHETER AND INTRODUCER
Conceptus, Inc.
MFD
Dec 27, 1994K933981CERVICAL CATHETER
Conceptus, Inc.
LKF
Dec 27, 1994K933723CONCEPTUS UTERINE CATHETER
Conceptus, Inc.
LKF

Latest recalls

DateFirm and productCodeLinked 510(k)
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