510(k) K827069
K827069 is an FDA 510(k) premarket notification submitted by Arrow X-Ray Corp. for the device "PODIOSCOPE BY ARROW". The FDA issued a decision of Substantially Equivalent on Feb 18, 1982. Arrow X-Ray Corp. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 18, 1982
- Date Received
- Jan 18, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No