510(k) K870284

TRIANGULAR BANDAGE by The Medical Group, Inc.

K870284 is an FDA 510(k) premarket notification submitted by The Medical Group, Inc. for the device "TRIANGULAR BANDAGE". The FDA issued a decision of Substantially Equivalent on February 24, 1987. The Medical Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 24, 1987
Date Received
January 27, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No