ACE ICPM SIDE PORTED NEEDLE
FDA 510(k) clearance K881858 · decided 1988-05-27
Clearance details
- K-number
- K881858
- Device name
- ACE ICPM SIDE PORTED NEEDLE
- Applicant
- Buckman Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-05-03
- Decision date
- 1988-05-27
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- LXC
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Martinez, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Buckman 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.