INSTAFIL
FDA 510(k) clearance K810795 · decided 1981-06-12
Clearance details
- K-number
- K810795
- Device name
- INSTAFIL
- Applicant
- Instafil, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1981-03-23
- Decision date
- 1981-06-12
- Days to decision
- 81 days
- Clearance type
- Traditional
- Product code
- KPE
- Device class
- 2
- Regulation number
- 880.5025
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Instafil
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.