SPERM SELECT SYSTEM
FDA 510(k) clearance K900308 · decided 1990-04-13
Clearance details
- K-number
- K900308
- Device name
- SPERM SELECT SYSTEM
- Applicant
- Pharmacia, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-01-22
- Decision date
- 1990-04-13
- Days to decision
- 81 days
- Clearance type
- Traditional
- Product code
- HDR
- Device class
- 2
- Regulation number
- 884.5250
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Piscataway, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| MODELS 011 & 011B IRIDOCAPSULAR IOLS (P810042) | Pharmacia, Inc. | 1982-12-15 |