PODIOSCOPE BY ARROW
FDA 510(k) clearance K827069 · decided 1982-02-18
Clearance details
- K-number
- K827069
- Device name
- PODIOSCOPE BY ARROW
- Applicant
- Arrow X-Ray Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-01-18
- Decision date
- 1982-02-18
- Days to decision
- 31 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Seattle, WA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Arrow X-Ray Corp.
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.