510(k) K832237

ORTHOPEDIC CASTING TAPE MAXCAST by Cutter Laboratories, Inc. — Product Code ITG

K832237 is an FDA 510(k) premarket notification submitted by Cutter Laboratories, Inc. for the device "ORTHOPEDIC CASTING TAPE MAXCAST". The FDA issued a decision of Substantially Equivalent on August 16, 1983. The device falls under product code ITG (Bandage, Cast), a Class I device regulated under 21 CFR 890.3025. Cutter Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1983
Date Received
July 11, 1983
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