510(k) K840416

HEXCELITE by Hexcel Medical — Product Code ITG

K840416 is an FDA 510(k) premarket notification submitted by Hexcel Medical for the device "HEXCELITE". The FDA issued a decision of Substantially Equivalent on March 23, 1984. The device falls under product code ITG (Bandage, Cast), a Class I device regulated under 21 CFR 890.3025. Hexcel Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 1984
Date Received
January 31, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bandage, Cast
Device Class
Class I
Regulation Number
890.3025
Review Panel
PM
Submission Type