510(k) K800279
K800279 is an FDA 510(k) premarket notification submitted by Medspec Corp. for the device "MEDSPEC RUBBER BANDS". The FDA issued a decision of Substantially Equivalent on May 2, 1980. Medspec Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 2, 1980
- Date Received
- February 5, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No