(15 days)
Not Found
No
The 510(k) summary describes a standard latex condom with no mention of AI or ML technology in its intended use, device description, or any other section.
No
The device is used for contraception and disease prevention, which are prophylactic purposes, not therapeutic interventions for existing conditions.
No
Explanation: The device description states its use is for contraception and prophylactic purposes, not for diagnosing any condition.
No
The device description clearly states it is a natural latex sheath, which is a physical hardware component.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to perform tests on samples taken from the human body (like blood, urine, tissue) to provide information about a person's health. These tests are performed outside of the body.
- Tulip Condom Function: The Tulip condom is a barrier device used on the body (specifically, on the penis) for contraception and disease prevention. It does not perform any tests on bodily samples.
The description clearly states its intended use is for contraception and prophylactic purposes, and its device description details its physical characteristics as a barrier. This aligns with the definition of a medical device, but not specifically an In Vitro Diagnostic.
N/A
Intended Use / Indications for Use
The Tulip condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted diseases).
The condom is used for contraception and for prophylactic purposes to help prevent pregnancy and the transmission of sexually transmitted diseases. If used properly, latex condoms will help to reduce the risk of transmission of HIV infection (AIDS) and many other sexually transmitted diseases including chlamydia infections, genital herpes, genital warts, gonorrhea, hepatitis B, and syphilis. In addition, this condom will help to reduce the risk of transmission of HIV infection (AIDS) and many other sexually transmitted diseases.
Product codes
85 HIS
Device Description
This condom is made of a natural latex sheath, which completely covers the penis with a closely fitted membrane. This condom is straight-walled with a reservoir tip, nominal length 180mm, nominal width 52mm, and nominal thickness 0.05mm. It is lubricated with silicon, with cornstarch as a dressing material. The condom is offered in natural latex color and is designed to conform to established American and international voluntary standards including ASTM D3492-02 and ISO 4074-1-1996.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies
Not Found
Key Metrics
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 884.5300 Condom.
(a)
Identification. A condom is a sheath which completely covers the penis with a closely fitting membrane. The condom is used for contraceptive and for prophylactic purposes (preventing transmission of sexually transmitted infections). The device may also be used to collect semen to aid in the diagnosis of infertility.(b)
Classification. (1) Class II (special controls) for condoms made of materials other than natural rubber latex, including natural membrane (skin) or synthetic.(2) Class II (special controls) for natural rubber latex condoms. The guidance document entitled “Class II Special Controls Guidance Document: Labeling for Natural Rubber Latex Condoms Classified Under 21 CFR 884.5300” will serve as the special control. See § 884.1(e) for the availability of this guidance document.
0
MAR 1 - 2005
Image /page/0/Picture/1 description: The image shows a sequence of handwritten alphanumeric characters. The characters appear to be "K050360D". The characters are written in a cursive style, and the image is in black and white.
SHANGHAI LATEX FACTORY
Abbreviated 510(k) for Male Latex Condoms
#K_
510(k) SUMMARY 川 .
| Submitted By: | Shanghai Latex Factory
1700, Huangxing road, Shanghai, China, 200433
Telephone: 0086-021-55090975
Fax: 0086-021-55061248 | | |
|------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|--|
| Contact Person: | Mr. Lou Ji | | |
| Date Prepared: | December 20, 2004 | | |
| Proprietary Name: | Tulip Condom | | |
| Common Name: | Latex Male Condom | | |
| Classification Name: | Condom (21 CFR 884.5300) | | |
| Predicate Device: | Latex Condom
510(k) #K[994118] | | |
| Description of Device: | This condom is made of a natural latex sheath, which completely covers the penis with a closely fitted membrane. This condom is straight-walled with a reservoir tip, nominal length 180mm, nominal width 52mm, and nominal thickness 0.05mm. It is lubricated with silicon, with cornstarch as a dressing material. The condom is offered in natural latex color and is designed to conform to established American and international voluntary standards including ASTM D3492-02 and ISO 4074-1-1996 | | |
1
Abbreviated 510(k) for Male Latex Condoms
સ મિ
This lates condom has the same intended use as the predicate Intended Use of the Device: The condom is used for contraception and for condom. prophylactic purposes to help prevent pregnancy and the transmission of sexually transmitted diseases. If used properly, latex condoms will help to reduce the risk of transmission of HIV infection (AIDS) and many other sexually transmitted diseases including chlamydia infections, genital herpes, genital warts, gonorrhea, hepatitis B, and syohilis. In addition, this condom will help to reduce the risk of transmission of HIV infection (AIDS) and many other sexually transmitted diseases.
Technological Characteristics: This condom has the same technological characteristics as the identified predicate condom above. The design İs 1 (1 conformance with ASTM Latex Condom Standard 03492 and that the condom is made of natural rubber latex. Accordingly, when compared to the predicate device, the tulip condom intended to be introduced does not incorporate any significant changes in the intended use, method of operation, materials, or design that could affect safety and effectiveness.
| Feature | Tulip Condom | Predicate Device |
|---|---|---|
| Length (mm) | 180 | 180 |
| Width (mm) | 52 | 52 |
| Thickness (mm) | 0.05 | 0.05 |
| Air Burst Pressure(kPa) | 2.3 | 2.4 |
| Air Burst Volume (dm³) | 38.5 | 36 |
| Lubricant System | Silicone | Silicone |
| Reservoir Tip | Yes | Yes |
2
Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the circle is an image of an eagle.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Shanghai Latex Factory % Ms. Laura L. Danielson Responsible Third Party Official 510(k) Program Manager TÜV Product Service 1775 Old Highway 8 NEW BRIGHTON MN 55112-1891 Re: K050360
MAR 1 - 2005
Trade/Device Name: Tulip Condom Regulation Number: 21 CFR 884.5300 Regulation Name: Condom Regulatory Class: II Product Code: 85 HIS Dated: February 11, 2005 Received: February 14, 2005
Dear Ms. Danielson:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced we have and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to the cherosate) to regulary ment date of the Medical Device Amendments, or to devices that have been recy 20, 1770, the chance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that recrassmod in accordal of a premarket approval application (PMA). You may, therefore, market the do not require to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your . In addition, be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to registration and listing (21 CFR Part 807), labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the clectronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
3
This letter will allow you to begin marketing your device as described in your Section 510(k) This letter will anow you to begin marketing of substantial equivalence of your device to a legally premarket notification. The FDA Inding of substantial organities and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), pleased on the regulation numer If you desire specific advice for your device on our labering regulation in the regulation number at the top of this letter:
| 21 CFR 876.xxxx | (Gastroenterology/Renal/Urology) | 240-276-0115 |
|---|---|---|
| 21 CFR 884.xxxx | (Obstetrics/Gynecology) | 240-276-0115 |
| 21 CFR 892.xxxx | (Radiology) | 240-276-0120 |
| Other | 240-276-0100 |
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Also, please note the regulation entired, "Nisoration on your responsibilities under the Act from the 807.97). You may obtain other general mannation on your of its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Nancy C. Hogdon
Nancy C. Brogdon Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
SHANGHAI LATEX FACTORY
Abbreviated 510(k) for Male Latex Condoms
માં આ
INDICATIONS FOR USE STATEMENT VII.
Indications for Use
K050360 510(k) Number (if known):
Device Name: Tulip Condom __
Indications For Use: The Tulip condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted diseases).
Prescription Use - - - -(Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) ...
Concurrence of CDRH, Otlice of Device Evaluation (ODE)
David R. Lyson
(Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices 510(k) Number
No. 1700, Huangxing Road, Shanghai, P.R.China
PAGE 16 / 16