510(k) K920905

BIOFORCE WIRE by Gac Intl., Inc. — Product Code DZC

K920905 is an FDA 510(k) premarket notification submitted by Gac Intl., Inc. for the device "BIOFORCE WIRE". The FDA issued a decision of Substantially Equivalent on November 4, 1992. 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
November 4, 1992
Date Received
February 27, 1992
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