DEXIDE LAPAROSCOPIC KITS
FDA 510(k) clearance K924117 · decided 1993-03-23
Clearance details
- K-number
- K924117
- Device name
- DEXIDE LAPAROSCOPIC KITS
- Applicant
- Dexide, Inc.
- Decision
- Unknown
- Date received
- 1992-08-14
- Decision date
- 1993-03-23
- Days to decision
- 221 days
- Clearance type
- Traditional
- Product code
- KDD
- Device class
- 1
- Regulation number
- 878.4800
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Fort Worth, TX, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Dexide
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.