Atlas FDA

SELECT IUI

FDA 510(k) clearance K954099 · decided 1995-11-22

Clearance details

K-number
K954099
Device name
SELECT IUI
Applicant
Select Medical Systems, Inc.
Decision
Substantially Equivalent
Date received
1995-08-31
Decision date
1995-11-22
Days to decision
83 days
Clearance type
Traditional
Product code
MFD
Device class
2
Regulation number
884.5250
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Williston, VT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
INSEMINATION CATHETER, MODEL 320301 (K021438)Labotect Labor-Technik Gottingen2002-07-16
THECURVE, ITEM 507 (K012935)Select Medical Systems, Inc.2001-10-11
`THE INSEMINATOR' (PROPOSED) (K984306)Wallach Surgical Devices, Inc.1999-03-01
MEDWORKS VISUALIZATION INSEMINATION CATHETER (K982630)Medworks Corp.1999-01-14
MEDWORKS INSEMINATION CATHETER (K982628)Medworks Corp.1998-08-21
EMBRYON INTRAUTERINE INSEMINATION CATHETER, EMRYON SOFT INTRAUTERINE INSEMINATION CATHETER, STYLET FOR EMBRYON INTRAUTER (K980061)Rocket Medical Plc1998-03-02
MINI-EMBRYON INTRA UTERINE INSEMINATION CATHETER (K972823)A & A Medical, Inc.1997-10-10
TOM CAT F.L., TOM CAT S.L. (K972245)A & A Medical, Inc.1997-08-06
MICROSPAN INSEMINATION SYSTEM (K970750)Imagyn Medical, Inc.1997-05-05
WALLACE ARTIFICIAL INSEMINATION CATHETER - 8CM/18CM (K964848)Marlow Surgical Technologies, Inc.1997-01-16
GENXCATHETER (K963031)Genx Intl., Inc.1996-10-21
MALLEABLE STYLET 18 CM ME1816ST, 23 CM ME1816NST (K962273)Marlo Surgical Technology1996-07-31

Recalls involving this device

No recalls on record reference this clearance.