DISPOSABLE INTRAUTERINE PRESSURE KIT MODEL 13972A
FDA 510(k) clearance K885316 · decided 1989-03-23
Clearance details
- K-number
- K885316
- Device name
- DISPOSABLE INTRAUTERINE PRESSURE KIT MODEL 13972A
- Applicant
- Hewlett-Packard Co.
- Decision
- Substantially Equivalent
- Date received
- 1988-12-29
- Decision date
- 1989-03-23
- Days to decision
- 84 days
- Clearance type
- Traditional
- Product code
- KXO
- Device class
- 2
- Regulation number
- 884.2700
- Medical specialty
- Obstetrics/Gynecology
- Advisory committee
- Obstetrics/Gynecology
- Location
- Andover, MA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Hewlett-Packard Co.
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.
Recalls involving this device
No recalls on record reference this clearance.