510(k) K851055

SENTINOL -ORTHODONTIC ARCH WIRE by Gac Intl., Inc. — Product Code DZC

K851055 is an FDA 510(k) premarket notification submitted by Gac Intl., Inc. for the device "SENTINOL -ORTHODONTIC ARCH WIRE". The FDA issued a decision of Substantially Equivalent on May 9, 1985. The device falls under product code DZC (Wire, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Gac Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1985
Date Received
March 14, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wire, Orthodontic
Device Class
Class I
Regulation Number
872.5410
Review Panel
DE
Submission Type