510(k) K837224
K837224 is an FDA 510(k) premarket notification submitted by Xanar, Inc. for the device "UNKNOWN". The FDA issued a decision of Substantially Equivalent on May 2, 1983. Xanar, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 2, 1983
- Date Received
- March 2, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No