SNOWDEN-PENCER IRRIGATION PUMP
FDA 510(k) clearance K920985 · decided 1992-06-09
Clearance details
- K-number
- K920985
- Device name
- SNOWDEN-PENCER IRRIGATION PUMP
- Applicant
- Snowden-Pencer
- Decision
- Substantially Equivalent
- Date received
- 1992-03-02
- Decision date
- 1992-06-09
- Days to decision
- 99 days
- Clearance type
- Traditional
- Product code
- HEI
- Device class
- 2
- Regulation number
- 884.2660
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Tucker, GA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Snowden-Pencer
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| DRG REACTION CHAMBER/SAFETY TIP (K012003) | Doctor'S Research Group, Inc. | 2002-02-12 |
| INNERVISION IRRIGATION PUMP (K910982) | M.D. Engineering, Inc. | 1991-08-26 |
Recalls involving this device
No recalls on record reference this clearance.