The following data is part of a premarket notification filed by Apex Medical Technologies, Inc. with the FDA for Polyurethane Condom.
| Device ID | K902936 |
| 510k Number | K902936 |
| Device Name: | POLYURETHANE CONDOM |
| Classification | Condom |
| Applicant | APEX MEDICAL TECHNOLOGIES, INC. 10064 MESA RIDGE CT., #202 San Diego, CA 92121 |
| Contact | Alice A Depaul |
| Correspondent | Alice A Depaul APEX MEDICAL TECHNOLOGIES, INC. 10064 MESA RIDGE CT., #202 San Diego, CA 92121 |
| Product Code | HIS |
| CFR Regulation Number | 884.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-07-03 |
| Decision Date | 1991-03-06 |