510(k) K800279

MEDSPEC RUBBER BANDS by Medspec Corp.

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