THE PATHFINDER
FDA 510(k) clearance K842304 · decided 1984-08-01
Clearance details
- K-number
- K842304
- Device name
- THE PATHFINDER
- Applicant
- Hydro-Med Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-06-11
- Decision date
- 1984-08-01
- Days to decision
- 51 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Hydro-Med Products
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.
Recalls involving this device
No recalls on record reference this clearance.