| Device |
kit, conception-assist, home use |
| Regulation Description |
Cervical cap. |
| Definition |
The kit is intended for assisted insemination in situations in which low sperm count , sperm immobility, or hostile vaginal environment have been diagnosed. The kit is used for semen collection and placement into the bowl of a cervical cap as an aid to conception. It is to be used at home following physician instruction. The Cap should not be left in place for more than 6 hours. The kit consists of: conception (cervical) caps; 3 polyurethane condoms; 24 ovulation predictors; 3 pregnancy test kits; 3 "sperm friendly" moisturizer samples (Pre Lubricant); 1 conception journal; 1 instruction manual; 2 conception wheels (1 in English and 1 in French); 1 medical provider envelope. |
| Physical State |
The Kit consists of : conception (cervical) caps (1 for practice insertions); 3 polyurethane condoms; 24 ovulation predictors; 3 pregnancy test kits; 3 "sperm friendly" moisturizer samples (Pre Lubricant); 1 conception journal; 1 instruction manual; 2 conception wheels (1 in English and 1 in French); 1 medical provider envelope. All device contents have been previously cleared through pre-market notifications; however, the condom and cervical cap have new indications for use (semen collector and collection cap respectively). |
| Technical Method |
During sexual intercouse, sperm is collected in a polyurethane semen collection device (condom). Immediately thereafter, this sperm is transferred to the bowl of a cervical cap (made of silicone elastomers). This cap is placed on the cervix for up to 6 hours, so as to improve the chances of insemination. |
| Target Area |
Sperm, uterine horn, vagina and embryo (if any) have the potential to be affected by this device. |
| Regulation Medical Specialty |
Obstetrics/Gynecology |
| Review Panel |
Obstetrics/Gynecology |
|---|
| Product Code | OBB |
|---|
| Premarket Review |
Reproductive, Gynecology and Urology Devices
(DHT3B)
Reproductive, Gynecology and Urology Devices
(DHT3B)
|
| Submission Type |
510(k)
|
|---|
| Regulation Number |
884.5250
|
|---|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
Summary Malfunction
Reporting |
Eligible |
| Implanted Device? |
No
|
|---|
| Life-Sustain/Support Device? |
No
|
|---|
| Third Party Review |
Not Third Party Eligible |
